JP5553148B2 - Affixing - Google Patents

Description

  The present invention relates to a patch such as a compress used to be applied to the skin surface of a human body, and particularly relates to a patch having a feature in its shape.

As a shape of the compress used for stiff shoulders, a rectangular shape is generally marketed.
The following patent document discloses an oval compress.

JP 2004-121784 A

In the invention of the patent document, the compress will be difficult to peel off.
However, the efficiency of cutting the poultice from the original fabric is significantly reduced.

  By the way, in the case of stiff shoulders, while removing the scapula site, covering the trapezius muscle (superficial muscle) and the large rhomboid muscle (deep muscle), and further applying a compress to cover the sternocleidomastoid muscle of the neck, The use efficiency of the compress is increased. For that purpose, it is necessary to put many small compresses, which is troublesome.

  On the other hand, when a large compress is applied, the large compress covers a portion of the scapula that does not need to be applied.

  There are many people who do not have knowledge about the position where the compress is applied. Therefore, the compress cannot be applied at an effective application position.

  Accordingly, an object of the present invention is to provide a paste such as a compress that does not require a large number of compresses, is less likely to be wasted, and has an easy-to-understand effective application position when stiff shoulders.

The patch of the present invention comprises an adhesive drug layer containing a drug to be applied to the skin surface of a human body, a support layer that supports the drug layer, and a release film that covers the drug layer application surface and is peeled off during use. a strip that can be taken successive raw shelled patches having a back portion covering the site between the shoulder blades and spine in trapezius extends upward along the spine, the back A pair of main parts integrally formed with a shoulder part covering the upper part of the scapula in the trapezius muscle, and covering the sternocleidomastoid muscle of the neck with a smaller area than the main part A pair of sub-parts suitable for the pair, the pair of main parts and the main part being at least partially in contact with each other and spaced apart at the remaining part, and the pair of sub-parts between the separated main part and main part In a state where they are in contact with each other and the main part and the sub part are in contact with each other. When a set pattern to take the raw shelled, repeat the set pattern, and to allow templating continuously, the shape of the main portion and the secondary portion is set.

Release film Another patch of the present invention, which is peeled off and the body of the contained drug put on the skin surface tackiness of the drug layer, a support layer supporting the drug layer, in use covers the drug layer application surface And a back part that can be cast from a continuous belt-like raw fabric comprising: a back part that extends upward along the spine and covers a portion of the trapezius between the scapula and the spine; A pair of L-shaped main portions integrally formed with a shoulder portion covering the portion of the trapezius above the scapula above the back portion, and a neck chest having a smaller area than the main portion. A pair of sub-parts suitable for covering the chain milking muscles, wherein the pair of main parts and main parts are adjacent to each other, and the sub-parts are arranged inside the corners of the L-type main parts. When the set pattern arranged in contact with the part is taken from the original fabric, the set pattern is repeated, One to allow templating continuously, the shape of the main portion and the secondary portion is set.

  According to the present invention, the main part of the patch does not cover the scapula and has a shape suitable for covering the trapezius muscle, while the sub part of the patch covers the sternocleidomastoid muscle of the neck. Since it is possible, it is only necessary to apply a total of four sheets of cloth on both the left and right sides. Therefore, waste of covering the scapula is less likely to occur, and less time is required for pasting.

  In addition, since the shape of the patch is not a square or an ellipse, and the main part has a substantially L-shaped or L-shaped shape, the person who purchased the patch pays attention to how to use the patch. Therefore, it can be expected that the instruction attached to the product or the explanation of the sticking position printed on the sticking sheet itself is read and the sticking is pasted in the correct position according to the explanation.

  In the present invention, the main portion includes a left main portion for covering the left trapezius muscle and a right main portion for covering the right trapezius muscle, and the pair of main portions are the left main portion and There are a case of the right main part, a case of only the left main part, and a case of only the right main part.

  That is, in one aspect, the pair of main parts includes a left main part for covering the left trapezius muscle and a right main part for covering the right trapezius muscle, and the left and right main parts are the same size. The pair of sub-parts have the same size and are symmetrical to each other.

  In this case, the left and right main parts are respectively attached to the left and right left trapezius muscles, and the pair of sub-parts are attached to the left and right neck sternocleidomastoid muscles. Therefore, stiffness of both trapezius muscles can be treated simultaneously with one set pattern.

  In another aspect of the present invention, the pair of main parts have the same size and shape, and both cover part of the left and right trapezius muscles, and the pair of sub-parts have the same size and shape.

  In this aspect, when there are two left main parts, one left main part and one sub part are pasted on the left side of the back and the left side of the neck. This set pattern is a set pattern for the left shoulder that is used for treatment of stiffness of the left shoulder.

  On the other hand, in the same mode, when there are two right main parts, one right main part and one sub part are pasted on the right side of the back and the right side of the neck. This set pattern is a set pattern for the right shoulder that is used for treatment of stiffness of the right shoulder.

  In the same mode, when treating the stiffness of the left and right shoulders, one set or the same number of set patterns for both the left shoulder and the right shoulder are prepared, and the left and right main parts and sub-parts are prepared from each set pattern. Take out and use.

In one aspect of the present invention, the pair of main parts and the pair of sub-parts are connected to each other in the release film, and are cut from each other in the drug layer and the support layer.

  In this aspect, since the drug layer and the support layer are cut in advance, it is easy for general consumers to use, and since one set pattern is connected to each other by the release film, the usage method is easy to understand.

In another aspect of the present invention, the pair of main portions and the pair of sub-portions are connected to each other in the release film, the drug layer, and the support layer, and the main films are provided on the release film and / or the support layer. A line that defines the boundary between the part and the sub part is printed.

  In this case, the patch is cut with scissors or the like at the time of use, so that it can be changed to a desired shape, and therefore, it will be suitable for specialists for scissors and manipulative treatment.

It is a rear view which shows arrangement | positioning of the compress as a patch of this invention with respect to a human body muscle and skeleton. It is a perspective view which shows the state which stuck the poultice concerning Example 1 of this invention. (A), (b) is the top view and sectional drawing which show the group pattern of the Example 1, (c) is the top view which shows the group pattern of Example 2. FIG. FIG. 3 is a plan view showing a method for producing the assembly pattern of Example 1. 6 is a plan view showing a manufacturing method of Example 2. FIG. It is a top view which shows the group pattern of the compresses concerning Example 3, and the method of manufacturing the same pattern. It is a top view which shows the method of manufacturing the group pattern concerning Example 4, and the group pattern of Example 3. (A), (b) is the top view and sectional drawing which show the group pattern of the compresses concerning Example 5, (c) is the top view which shows the group pattern of Example 6. FIG. (A) And (b) is a top view which shows the group pattern of Example 7 and 8, respectively. It is a top view which shows the modification of the set pattern of the compress according to Example 2. It is explanatory drawing which shows an example of the state which stuck the conventional commercially available compress. It is explanatory drawing which shows an example of the state which affixed the compress of this invention. It is explanatory drawing which shows the other example of the state which affixed the conventional commercially available compress. It is explanatory drawing which shows the further another example of the state which stuck the conventional commercially available compress. It is explanatory drawing which shows the other example of the state which affixed the compress of this invention. It is explanatory drawing which shows the further another example of the state which affixed the compress of this invention.

  Prior to the description of the embodiments of the present invention, the relationship between stiff shoulders and migraines and human muscles will be briefly described.

  In FIG. 1, M1 is a trapezius muscle, M2 is a sternocleidomastoid muscle, and in this figure, only the left mitral muscle M1 and the sternocleidomastoid muscle M2 are shown. The trapezius muscle M1 is a superficial muscle, and the trapezius muscle M1 covers a large rhomboid muscle (not shown) which is a deep muscle.

  B1 is the spine (spine) and B2 is the scapula. The scapula B2 is supported by the trapezius muscle M1 and the rhomboid muscle. The trapezius muscle M1 and the sternocleidomastoid muscle M2 extend to the lower back of the occipital region or temporal region. When these muscles become stiff, they feel stiff shoulders, and when the stiff shoulders advance, I feel migraines because of a bad flow.

  By applying a poultice having a medicinal effect component to a portion corresponding to the trapezius muscle M1 or the sternocleidomastoid muscle M2, muscle stiffness is loosened and shoulder stiffness and migraine symptoms are eased. On the other hand, even if the compress is applied to the portion of the scapula B2 that is not covered with the trapezius muscle M1, the effect cannot be obtained.

Examples of the present invention will be described below.
A poultice as an adhesive in this embodiment is used as shown in FIGS.

Example 1:
As shown in FIG. 3B, the poultice of Example 1 includes an adhesive drug layer Me containing a drug to be applied to the skin surface of the human body, a support layer S that supports the drug layer Me, and the drug layer Me. And a release film F that covers the sticking surface Mf and is peeled off during use.

  The application surface Mf of the drug layer Me adheres to the skin surface. The support layer S may be a nonwoven fabric having air permeability and / or stretchability, for example. The release film F is peeled off during use.

  As shown in FIG. 3A, the pack pattern P1 of the present embodiment includes a left main portion 1L, a right main portion 1R, a left sub portion 2L, and a right sub portion 2R.

  In the pack of this set pattern P1, the pair of main portions 1L, 1R and the pair of sub-portions 2L, 2R are connected to each other in the release film F, and the cutting line CL of the drug layer Me and the support layer S Are cut from each other. Therefore, each main part 1L, 1R and each sub part 2L, 2R can be used by peeling off the drug layer Me and the support layer S from the release film F individually (applying to the human body).

  In the set pattern P1, the pair of main portions 1L and 1R includes a left main portion 1L for covering the left trapezius muscle M1 and a right main portion 1R for covering the right trapezius muscle, and the left and right main portions. 1L and 1R have the same size and are symmetrical with respect to the cutting line CL. Each of the main parts 1L and 1R is formed by integrally forming a back part 11 and a shoulder part 12 respectively. Referring to the right main portion 1R of FIG. 1 as a representative, the back portion 11 extends upward along the spine B1 and covers a portion of the trapezius muscle M1 between the scapula B2 and the spine B1. The shoulder 12 covers a portion of the trapezius M1 above the scapula B2 above the back 11.

  The sub-parts 2L and 2R in FIG. 3 are symmetrical with respect to the cutting line CL, and have the same size. The right sub-portion 2R in FIG. 1 will be described as a representative example. The right sub-portion 2R has a substantially crescent-shaped or substantially boomerang-shaped shape suitable for covering the sternocleidomastoid muscle M2 of the neck, and the main portions 1L, 1R. Have a smaller area.

  In FIG. 3A, the pair of main portions 1L and 1R is partly in contact with each other and separated from each other in the remaining portion, and between the separated main portions 1L and 1R, The left main portion 1L and the left sub portion 2L are in contact with each other while the pair of sub portions 2L and 2R are in contact with each other, and the right main portion 1R and the right sub portion 2R are in contact with each other. ing.

In the set pattern P1, the vertical boundary line Cp in each of the main portions 1L and 1R is formed point-symmetrically about the vertical center point O. Therefore, as will be described later, it is possible to mold the set pattern P1 continuously from the original fabric without waste.

  Next, a method of manufacturing the compress of the set pattern P1 will be described.

  First, the support layer S, the drug layer Me, and the release film F are laminated, and the raw fabric W of FIG. 4 that is not cut is generated. Next, the support layer S and the drug layer Me other than the release film F are cut along the cutting line CL at each boundary between the main portions 1L and 1R and the sub-portions 2L and 2R for each set pattern P1. Thereafter, the support layer S, the drug layer Me, and the release film F, that is, the original fabric W are cut at the boundary line Cp of each set pattern P1.

  Here, in the poultice of the main set pattern P1, the boundary line Cp is formed point-symmetrically around the center point O in the boundary line Cp of the adjacent set pattern P1. Thus, since the shapes of the main portions 1L and 1R and the sub-portions 2L and 2R are set, when the set pattern P1 of the present invention is taken from the original fabric W, the set pattern is repeated, and The mold can be taken continuously without substantial waste.

  The main parts 1L and 1R and the sub parts 2L and 2R in FIG. 3 thus manufactured are the trapezius M1 and the sternocleidomastoid muscle M2 as shown by the right main part 1R and the right sub part 2R in FIGS. Affixed to cover. At this time, since it is not affixed essentially to the portion of the scapula B2 where the trapezius muscle M1 does not exist, the treatment efficiency is increased.

  Furthermore, each main part 1L and 1R is affixed so that a spine part may not be covered. The spinal nerve passes through the spinal portion, but the portion through which the spinal nerve passes is not cooled, so that side effects such as nerve block do not occur.

  Moreover, since the shape of each main part 1L and 1R is a shape close | similar to L type | mold, a sticking position is easy to understand.

  In the following, in the other embodiments, portions different from the above embodiments will be mainly described, and the same or corresponding portions as those in the above embodiments will be denoted by the same reference numerals, and description thereof will be omitted.

Example 2:
FIG. 3C and FIG. 5 show Example 2.
The set pattern P2 in FIG. 3C is rectangular and includes a left set pattern PL and a right set pattern PR.

  The left set pattern PL is composed of a pair of left main portions 1L having the same shape and size, and a pair of left sub-portions 2L having the same shape and size, and is formed in a square shape. The right set pattern PR is composed of a pair of right main portions 1R having the same shape and size, and a pair of right sub-portions 2R having the same shape and size, and is formed in a square shape. The left set pattern PL and the right set pattern PR are formed point-symmetrically around the center point O1 above and below the cutting line CL between the pair of main portions 1L, 1R. The boundary line Cp of the set pattern 2 is formed point-symmetrically with respect to the center point O.

  As shown in FIG. 5, the set pattern P2 of the present embodiment is obtained by die-cutting the support layer S and the drug layer Me along the cutting lines CL along the three-layer raw fabric W, and then cutting lines indicated by virtual lines. The pattern is cut for each set pattern P2 along Lr.

Example 3:
FIG. 6 shows a third embodiment.
The set pattern P2 may be divided into a left set pattern PL and a right set pattern PR as shown in FIGS. The left set pattern PL and the right set pattern PR can be used for the left shoulder and the right shoulder, respectively, and the left set pattern PL and the right set pattern PR divided into the two are individually wrapped as one set pattern P2. May be sold.

  The compresses separated into the left set pattern PL and the right set pattern PR can be cut out from the original fabric by various methods because the left set pattern PL and the right set pattern PR are each rectangular. For example, the compresses separated into the left set pattern PL and the right set pattern PR may be alternately taken out from a narrow original fabric W as shown in FIG.

Example 4:
FIG. 7 shows a fourth embodiment.
In the fourth embodiment, the set patterns PL and PR are separated from each other, but the main portions 1L and 1R and the sub portions 2L and 2R in the set patterns PL and PR are the support layer S, the drug layer Me, and In the peeling film F, it is mutually connected.

  Instead of providing the cutting line CL of the first to third embodiments, the line L is formed on the release film F as shown by a broken line so that the user can cut each part 1L, 1R, 2L, 2R by scissors or the like. It is printed. In this case, the treatment specialist can divide the main parts 1L and 1R and the sub parts 2L and 2R into optimal shapes.

  That is, the pair of main portions 1L and 1R and the pair of sub-portions 2L and 2R are connected to each other in the release film F, the drug layer Me, and the support layer S, and the release film F and / or the support layer S. A line L that defines the boundary between the main parts 1L and 1R and the sub-parts 2L and 2R is printed.

8A and 8B show the fifth embodiment.
In the fifth embodiment, the left main portion 1L and the right main portion 1R are adjacent to each other and are in contact with each other in almost all of the cutting lines CL, and are arranged symmetrically with respect to each other about the cutting line CL. In this embodiment, each main part 1L, R is generally L-shaped.

  Inside the corners of the main portions 1L and 1R, for example, crescent-shaped sub-portions 2L and 2R are arranged. The boundary line Cp of the set pattern P3 is formed point-symmetrically around the center point O on the boundary line Cp of each of the sub-parts 2L and 2R.

  In Example 1 of FIG. 3A, for example, boomerang-type sub-parts 2L and 2R are disposed outside the corners of the main parts 1L and 1R.

FIG. 8C shows the sixth embodiment.
In the embodiment of FIG. 8C, one set pattern PR is formed by two sets of the right main portion 1R and the right sub portion 2R. Each right main portion 1R and each right sub-portion 2R are formed symmetrically with respect to each other about the center point O.

  As shown in FIGS. 9A and 9B, the right sub-portion 2R may have a substantially triangular shape or the like.

FIG. 10 shows a modification of the second embodiment.
In the modification of the second embodiment, it is formed in the same manner as the set pattern P2 of the second embodiment, and a pair of left main portions 1L and a pair of left sub-portions 2L of the left set pattern PL, and a right set pattern PR. The pair of right main portions 1R and the pair of right sub portions 2R are formed by rounding all corners located on the outer periphery of the square shape.

As described above, the preferred embodiments have been described with reference to the drawings. However, those skilled in the art will readily understand various changes and modifications within the obvious scope by looking at the present specification.
For example, the crescent moon type or boomerang type sub-part may be divided into two.
The usage method may be printed on the main film or the like.
Accordingly, such changes and modifications are to be construed as within the scope of the invention as defined by the claims.

  Next, the effect of alleviating stiff shoulder symptoms when using a poultice as a patch of the present invention will be described.

  As a method for subjectively evaluating a person's pain intensity, a test called a visual analog scale (hereinafter referred to as “VAS”) is known.

  In order to carry out this VAS, the numerical value is measured before applying the compress and after applying the compress. For example, when the stiff shoulder symptom is strongest, “10” is set, and when there is no stiff shoulder symptom, “0” is set, and the sensation of the stiff shoulder symptom is digitized in 11 stages.

  In this case, the greater the effect of mitigating stiff shoulder symptoms, the greater the difference between the value of the stiff shoulder symptom of the subject before applying the compress and the value of the stiff shoulder symptom of the subject after applying the compress. It is an index of the relief effect of stiffness symptoms.

  Therefore, a questionnaire survey on the following use results was performed on 176 subjects who answered “10” and 306 subjects who answered “7” as the numerical value of stiff shoulder symptoms before applying the compress.

176 subjects who answered “10” and 306 subjects who answered “7” were divided into two groups of 88 and 153, respectively. Commercially available compresses V (square shape: 14 cm × 10 cm = 140 cm ² ) are pasted on the left and right sides of the spine, respectively, and the other set has a pair of main parts 1L of the compresses of the present invention as shown in FIG. , 1R (135cm ² ) is applied to the left and right sides of the spine, both are applied for 2 hours and then removed, and after another 8 hours, both are applied for 2 hours in the same manner and then removed. It was.

  Each subject was asked to answer the stiff shoulder symptom the next day, 3 days, and 1 week after applying the compress, and the difference was tabulated to obtain the results shown in Table 1 below. It was.

  According to Table 1, in the test subjects who answered “10”, the compress of the present invention had an average per capita value that was 0.50 points larger on the next day than the commercially available compress, and 0.82 points greater after three days. After a week, the result was 1.17 points larger. In the test subjects who answered “7”, the compress of the present invention was an average value per person, which was 0.48 points larger on the next day, 0.87 points greater on the third day, and one week later than the commercially available compress. The result was 1.10 points larger.

  Therefore, it can be said that the compress as the patch of the present invention is superior in the effect of alleviating the stiff shoulder symptom compared to the commercially available compress.

  Furthermore, the effect of alleviating complications (symptoms other than stiff shoulders) when using the poultice as the patch of the present invention will be described.

  Examples of complications include headache, nausea, irritability, depression, anorexia, bulimia, sleep disorders, toothache, tinnitus, dizziness, and eye strain.

  Therefore, among the 274 subjects who replied "9" as the numerical value of the stiff shoulder symptom before applying the compress in the VAS test, 252 subjects with complications were subjected to a questionnaire survey on the following use results. .

Each of the 252 subjects was divided into four groups of 63, and the first group had a conventional rectangular compress W (165 cm ² ) attached to the left and right sides of the spine, as shown in FIG. As shown in FIG. 13, the eyes have six conventional rectangular compresses X (55 cm ² ) attached to the left and right sides of the shoulder and spine, and the third set is shown in FIG. As described above, a pair of main portions 1L, 1R and sub-portions 2L, 2R (165 cm ^{2 of} each main portion and sub-portion are combined) of the poultice of the present invention, and these sub-portions 2L, 2R are Attached to the upper part of the trapezius muscles, the lower part of the trapezius muscles is attached to the main parts 1L and 1R of the compresses. As shown in FIG. part 1L, 1R and auxiliary portions 2L, 2R (165cm ² together each main portion and secondary portion) Use, have these main parts 1L and 1R attached to the left and right trapezius muscles of the spine, and have the accessory parts 2L and 2R attached to the left and right sternocleidomastoid muscles, both of which are applied for 2 hours and then removed In addition, after 8 hours, they were applied again for 2 hours in the same manner, and then peeled off.

  And when each subject asked whether or not the complications were eased even a little after one week after applying the compress, 29 respondents (46%) answered that it became easy, and in the second set, Forty-six (73%) responded that it became easier, 58 (92%) said that it became easier in the third group, and 59 (94%) said that it became easier in the fourth group.

  Therefore, it can be said that the compress as the patch of the present invention is superior in the effect of alleviating complications as compared with a commercially available compress.

  Finally, the results of examining the ease of movement and the presence or absence of discomfort when using the poultice as the patch of the present invention will be described.

As shown in FIG. 10, the numerical value of the stiff shoulder symptom before applying the compress in the VAS test is “8”. As shown in FIG. 10, the conventional commercially available compress V (square-shaped compress: 14 cm × 10 cm = 140 cm ² ) on the left and right sides of the spine, and as shown in FIG. 11, the pair of main parts 1L, 1R (140 cm ² ) of the compresses were put on the left and right sides of the spine, respectively. When comparing the ease of movement and discomfort, 138 (92%) answered that the compress of the present invention was “easy to move” or “no discomfort”.

  Therefore, it can be said that the poultice as the patch of the present invention is superior in terms of easiness of movement and a sense of incongruity compared to a commercially available poultice.

  The patch of the present invention can be used as a hot compress or a cold compress for treatment of stiff shoulders, to fix joints, muscles, etc., and to taping as an emergency measure in case of sprain or fracture.

11: Back part 12: Shoulder part B1: Spine B2: Scapula M1: Trapezius M2: Sternocleidomastoid muscle F: Release film Me: Drug layer Mf: Attached surface 1L: Left main part 1R: Right main part 2L: Left sub-portion 2R: Right sub-portion S: Support layer P1: Assembly pattern CL: Cutting line Cp: Boundary line O: Center point W: Original fabric

Claims (6)

A belt-like continuous raw material comprising an adhesive drug layer containing a drug to be applied to the skin surface of a human body, a support layer for supporting the drug layer, and a release film that covers the drug layer application surface and is peeled off during use. a patch that can be taken anti shelled,
A back that extends upward along the spine and covers a portion of the trapezius between the scapula and the spine; and a shoulder that covers a portion of the trapezius above the scapula above the back. A pair of main parts integrally formed;
A pair of sub-parts suitable for covering the sternocleidomastoid muscle of the neck with an area smaller than the main part,
The pair of main portions and the main portions are at least partially in contact with each other and spaced apart from each other;
When a pair of sub-parts are in contact with each other between the separated main part and main part, and a set pattern arranged in a state in which the main part and sub-part are in contact with each other is molded from the original fabric In addition, the shape of the main part and the sub part is set so that the set pattern can be repeated and continuously formed. A belt-like continuous raw material comprising an adhesive drug layer containing a drug to be applied to the skin surface of a human body, a support layer for supporting the drug layer, and a release film that covers the drug layer application surface and is peeled off during use. a patch that can be taken anti shelled,
A back that extends upward along the spine and covers a portion of the trapezius between the scapula and the spine; and a shoulder that covers a portion of the trapezius above the scapula above the back. A pair of L-shaped main parts integrally formed;
A pair of sub-parts suitable for covering the sternocleidomastoid muscle of the neck with an area smaller than the main part,
The pair of main portions and main portions are adjacent to each other;
In the case where a set pattern in which each sub-part is arranged in contact with the main part inside the corner of each L-shaped main part is molded from the original fabric, the set pattern is repeated and continuously. A patch in which the shapes of the main part and the sub part are set so that the mold can be taken. 3. The pair of main parts according to claim 1, wherein the pair of main parts includes a left main part for covering the left trapezius and a right main part for covering the right trapezius, and the left and right main parts are the same. Size and symmetrical shape to each other,
The pair of sub-parts is the same size as each other, and a sticking cloth having a symmetrical shape. The pair of main parts according to claim 1 or 2, wherein the pair of main parts have the same size and shape, and both cover part of the left and right trapezius muscles,
The pair of sub-parts is a patch having the same size and shape.   The patch according to any one of claims 1 to 4, wherein the pair of main parts and the pair of sub parts are connected to each other in the release film and are cut from each other in the drug layer and the support layer.   In any one of Claims 1-4, the said pair of main part and a pair of sub part are mutually connected in the said peeling film, a chemical | medical agent layer, and a support layer, and each said to a release film and / or a support layer A patch printed with a line that defines the boundary between the main part and the sub part.

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