JPS6016909A - Water-based cosmetic - Google Patents
Water-based cosmeticInfo
- Publication number
- JPS6016909A JPS6016909A JP12377083A JP12377083A JPS6016909A JP S6016909 A JPS6016909 A JP S6016909A JP 12377083 A JP12377083 A JP 12377083A JP 12377083 A JP12377083 A JP 12377083A JP S6016909 A JPS6016909 A JP S6016909A
- Authority
- JP
- Japan
- Prior art keywords
- water
- formula
- product
- mono
- based cosmetic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0216—Solid or semisolid forms
- A61K8/0229—Sticks
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
- A61K8/498—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin
Abstract
Description
【発明の詳細な説明】
本発明は水系化粧料に関し、更に詳しくはゲル状乃至固
形状の水系化粧料に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a water-based cosmetic, and more particularly to a gel-like or solid-based water-based cosmetic.
従来、水系のゲル化剤としては天然あるいは合成の水溶
性高分子加合物が知られている。しかしながら、水を固
化するためには水溶性高分子濃度なかなり高くしなけれ
ばならず−また固化できたとしても、それを口紅のよう
なスティック状化粧料として使用できるほどの折れ強度
にすることは難しい・このため・水系のスティック状化
粧料は現在のところ見当らない。Conventionally, natural or synthetic water-soluble polymer adducts have been known as water-based gelling agents. However, in order to solidify water, the concentration of water-soluble polymers must be quite high - and even if it can be solidified, it must be strong enough to bend so that it can be used as a stick cosmetic such as lipstick. This is difficult, and for this reason, there are currently no water-based stick cosmetics available.
本発明者らは、上述したゲル状乃至固形状の水系化粧料
を得るためのゲル化剤に関して種苛検討を行なった結果
、特定の芳香族アルデヒドと多価アルコールとの縮合物
を特定割合で組み合せたならば、良好に水をゲル化する
ことが可能であり、もって新規な形態を有し保存安定性
にも優れたゲすなわち、本発明は、(1)式で示される
化合物の1種又は2種以上と、(■)式で示される化合
物の1種又は2種以上とを含有することを特徴とする水
系化粧料である・
HH
(1)式 (II)式
(式中、Rは水素原子、カルボキシル基、炭素数1〜3
のアルキル基、アルキル部分の炭素数が1〜3のアルコ
キシ基から選ばれた原子又は基を表わし、nは1又は2
の整数を示す。)
(以下余白)
本発明で用いられる(Ij式で示される化合物及び(I
f)式で示される化合物は芳香族アルデヒドと炭素数5
及び6の多価アルコールとの縮合物で、(I)式で示さ
れる縮合物はモノ体、(Il)式で示される縮合物はジ
体である。以下、(I)式で示される化合物をモノ体、
(■)式で示される化合物をジ体と呼ぶ。The present inventors conducted extensive research on gelling agents for obtaining the above-mentioned gel-like or solid water-based cosmetics. When combined, it is possible to gel water well, and has a novel form and excellent storage stability. HH (1) formula (II) formula (wherein, R is hydrogen atom, carboxyl group, carbon number 1-3
represents an atom or group selected from an alkyl group, an alkoxy group whose alkyl moiety has 1 to 3 carbon atoms, and n is 1 or 2.
indicates an integer. ) (hereinafter blank) The compound represented by the formula (Ij) used in the present invention and (I
f) The compound represented by the formula is an aromatic aldehyde and has 5 carbon atoms.
and 6 with a polyhydric alcohol, the condensate represented by formula (I) is a mono-form, and the condensate represented by formula (Il) is a di-form. Hereinafter, the compound represented by formula (I) will be described as a monomer,
The compound represented by the formula (■) is called a di-form.
ジベンジリデン−D−ソルビトールは上記ジ体の代表的
なもので、従来、油溶性のゲル化剤として知られている
。Dibenzylidene-D-sorbitol is a typical example of the above-mentioned di-isomer and is conventionally known as an oil-soluble gelling agent.
本発明者らは、このようなジ体とモノ体とを特定糸
比率において組合せることによって水≠のゲル化を可能
にし、その結果、従来の水系化粧料にはないゲル状乃至
固形状の水系化粧料を完成するに至ったのである。The present inventors have made it possible to gel water≠ by combining such di-bodies and mono-bodies at a specific thread ratio, and as a result, they have created gel-like or solid-type products that are not found in conventional water-based cosmetics. This led to the completion of water-based cosmetics.
上記モノ体、ジ体の配合量は、モノ体及びジ体の総量と
して本発明の水系化粧料全量中の0.1重量%(以下、
単に%と称す)及至20%であるが、モノ体とジ体の割
合が90 : 10及至10 : 90 (重量比)、
より好ましくは’75 : 25及至25 : ’75
(重量比)の範囲である。ジ体の割合が少ない程、系
の透明性は良くなる傾向がある。The blending amount of the above-mentioned mono- and di-forms is 0.1% by weight (hereinafter referred to as
(simply referred to as %) to 20%, but the ratio of mono-isomer to di-isomer is 90:10 to 10:90 (weight ratio),
More preferably '75: 25 to 25: '75
(weight ratio). The lower the proportion of di-isomer, the better the transparency of the system tends to be.
本発明の水系化粧料とは水を含有する化粧料であって、
その剤型は問わない。すなわち、透明可溶化系、乳液、
クリーム等の乳化系(油中水型、水中油型)あるいはさ
らにこれらに粉末を分散した粉末分散系専横々な剤型を
取ることができる。The aqueous cosmetic of the present invention is a cosmetic containing water,
The dosage form does not matter. That is, transparent solubilized systems, emulsions,
A variety of formulations can be used, including emulsion systems such as creams (water-in-oil type, oil-in-water type), or powder dispersion systems in which powder is further dispersed in these emulsions.
水の含有量は一般的に本発明の水系化粧料全量中の5〜
99.9%である。The water content is generally 5 to 5% of the total amount of the water-based cosmetic of the present invention.
It is 99.9%.
又、製品形状としても、流動性を有するゲル状及至非動
性のゲル状の製品から固形状の製品まで巾広い形状をと
ることができる、ゲル状の場合はチューブ容器やクリー
ム容器等に充填したり、固形状の場合はスチ、7り状に
成型したり、中皿に充填したりして使用する。In addition, the product shape can take a wide range of shapes, from fluid gel-like products to immobile gel-like products to solid products. In the case of gel-like products, they can be filled into tube containers, cream containers, etc. If it is in solid form, it can be molded into a strip, or filled into a medium dish.
これら様々な剤型、様々な製品形状の中では、水中油型
乳化系及至は透明可溶化系が従来の化粧料に比較して形
態的に新規性が強く、その中でもスチ、2り状のものが
従来全くなかった形状の製品として商品価値が高い。Among these various dosage forms and product shapes, oil-in-water emulsion systems and transparent solubilized systems are more novel in form than conventional cosmetics. It has a high commercial value as it has a shape that has never existed before.
前記モノ体、ジ体は前記特定割合、特定配合量の範囲内
で、そのまま本発明の水系化粧料に配合することができ
るが、N−メチルピロリドン、N、N−ジメチルアセト
アミド、シクロヘキサノン、モルホリン等の助溶剤中に
あらかじめ溶解しておいてから後、前記水系化粧料に添
加すればさらに容易に溶解させることができる。The above-mentioned mono- and di-forms can be incorporated into the aqueous cosmetics of the present invention as they are within the specified proportions and amounts, but N-methylpyrrolidone, N,N-dimethylacetamide, cyclohexanone, morpholine, etc. It can be further easily dissolved by pre-dissolving it in a co-solvent and then adding it to the water-based cosmetic.
本発明の水系化粧料には上記必須構成成分に加えて必要
に応じて、ポリビニルアルコール、カルボキシビニルポ
リマー等の合成水溶性高分子・セルロース誘導体、アラ
ビアゴム等の天然水溶性高分子、M分、防腐剤、殺菌剤
、金属イオン封鎖剤、香料、紫外線吸収剤、染料、顔料
、粉末、保湿剤、されなi−+ればならない。In addition to the above-mentioned essential components, the aqueous cosmetic of the present invention may optionally contain synthetic water-soluble polymers such as polyvinyl alcohol, carboxyvinyl polymers, cellulose derivatives, natural water-soluble polymers such as gum arabic, M content, Preservatives, bactericidal agents, sequestrants, perfumes, ultraviolet absorbers, dyes, pigments, powders, humectants, and other substances must be present.
次に実施例によって本発明をさらに詳細に説明する。本
発明はこれによって限定されるものではない。Next, the present invention will be explained in more detail with reference to Examples. The present invention is not limited thereby.
実施例1
第1表の成分を混合し、70°Cに加温して溶解後広口
瓶に入れて30’Cまで冷却した。得られたゲルの硬度
を第1表に示す。Example 1 The ingredients shown in Table 1 were mixed, heated to 70°C, dissolved, and then placed in a wide-mouthed bottle and cooled to 30'C. Table 1 shows the hardness of the gel obtained.
実施例1〜9は良好なゲルを生成し硬度が出るのに対し
て、モノ体あるいはジ体のみの比較例1゜2は良好なゲ
ルができなかった0
×1 レオメータ−(不動工業) 針6φ上昇速度2c
m/nunX2 ゲル化しない
X3 均一なゲルにならない
(実施例]−0) 透明水系口紅
精 製 水 to :too%
グリセリン 5
ポリビニルアルコール 1
モノベンジリデン−D−ソルビトール(モノ体)2ジベ
ンジリデン−D−ソルビトール(ジ体)2染 料 適量
防腐剤
香 料
ポリビニルアルコールとグリセリンを溶解した精製水を
60〜706Cに加温し、この中にモノ体とジ体を添加
して溶解する。これに染料、防腐剤、香料を溶解後、所
定の容器に流し込み、冷却固化させた。こうして得られ
た透明の水系口紅は全く新しいタイプの口紅で、従来の
油性口紅に比較するとベタつきがなく使用性に優れ、且
つ外観が透明であるという特長を有する従来にない口紅
であった0
0
(実施例11 ) ゲル状化粧水
精 製 水 to IOQ%
エタノール 10
PEG−(500”
グリセリン
モノベンジリデンキシリトール(モノ体) 0.9ジベ
ンジリデン−D−ソルビトール(ジ体) O,1LPO
E (20モル)ソルビタンモノラウレート 1香 料
01
染 料 001
防腐剤、紫外線吸収剤 適量
エタノール、PKG−1500、グリセリン、POE(
20モル)ソルビタンモノラウレートを溶解しり精製水
を50〜60°Cに加温し、これGこモノ体とジ体を添
加して溶解する0これに香料、染料、防腐剤、紫外線吸
収剤を溶解後、所定の容器Gこ流し込み冷却固化させた
。こうして得られたゲル状イヒ粧水(ま従来にないタイ
プの化粧水で・塗布しやすく、携帯性も便利であった。Examples 1 to 9 produced good gels and hardness, whereas Comparative Examples 1 and 2, which contained only mono- or di-forms, did not produce good gels. 6φ rising speed 2c
m/nunX2 Does not gel Sorbitol (di-isomer) 2 Dye Appropriate amount Preservative Flavor Purified water in which polyvinyl alcohol and glycerin have been dissolved is heated to 60-706C, and the mono-isomer and di-isomer are added thereto and dissolved. After dissolving the dye, preservative, and fragrance, the solution was poured into a predetermined container and solidified by cooling. The transparent water-based lipstick thus obtained was a completely new type of lipstick, and compared to conventional oil-based lipsticks, it was non-sticky, easy to use, and had a transparent appearance. (Example 11) Purification of gel-like lotion Water to IOQ% Ethanol 10 PEG-(500” Glycerin monobenzylidene xylitol (mono form) 0.9 dibenzylidene-D-sorbitol (di form) O,1LPO
E (20 mol) Sorbitan monolaurate 1 Fragrance 01 Dye 001 Preservative, UV absorber Appropriate amount Ethanol, PKG-1500, Glycerin, POE (
Dissolve sorbitan monolaurate (20 moles), heat purified water to 50-60°C, add and dissolve G-mono-isomer and di-isomer, and add fragrances, dyes, preservatives, and ultraviolet absorbers to this. After dissolving, the mixture was poured into a predetermined container G and cooled and solidified. The resulting gel-like lotion (well, a type of lotion that had never existed before) was easy to apply and convenient to carry.
1−1
(実施例]2) 水溶性ポマード
精 製 水 to 100%
流動パラフィン 5
オリーブ油 3
POEセチルエーテル 10
F’EG−15005
千ノベンジリデンアラビトール(モノ体)1ジベンジリ
デンアラビトール(ジ体) 2N−メチルピロリドン
6
香 料 適量
染 料
防腐剤、酸化防止剤
精製水にPOEセチルエーテルを溶解し、さらに油分、
その他の成分を溶解する。この中にモノ体とジ体を溶解
したN−メチルピロリドンを60″Cで添加し、冷却固
化させた。こうして得られた水溶性ポマードは従来のも
のより透明性に優れ、また広い温度範囲で安定であった
。1-1 (Example) 2) Water-soluble pomade purification Water to 100% Liquid paraffin 5 Olive oil 3 POE cetyl ether 10 F'EG-15005 1,000 nobenzylidene arabitol (mono form) 1, dibenzylidene arabitol (di form) 2N-methylpyrrolidone
6 Fragrance Appropriate amount Dye Preservative, antioxidant Dissolve POE cetyl ether in purified water, and add oil,
Dissolve other ingredients. N-methylpyrrolidone in which the mono- and di-isomers were dissolved was added at 60"C and solidified by cooling. The water-soluble pomade thus obtained has better transparency than conventional pomades and can be used in a wide temperature range. It was stable.
?8111]RGO−IG909 (4)(実施例]3
) クリームシャンプー
ラウリルジェタノールアミド 5
グリセリン z5
1.3ブチレングリコール a5
エチレングリコール七ノステアリン酸エステル 3N−
メチルピロリドン 3
モノ(メチルベンジリデン)−D−ソルビトール(モノ
体) 0.2ジ(メチルベンジリデン)−D−ソルビト
ール(ジ体) 0.1精製水 to 100
染料、香料、防腐剤、金属イオン封鎖剤 適量モノ体及
びジ体を溶解したN−メチルピロリドンを60〜70°
Cで精製水に加え溶解後、他の成分を加えて溶解する。? 8111] RGO-IG909 (4) (Example) 3
) Cream shampoo lauryl jetanolamide 5 Glycerin z5 1.3 butylene glycol a5 Ethylene glycol heptanostearate 3N-
Methylpyrrolidone 3 Mono(methylbenzylidene)-D-sorbitol (mono form) 0.2 Di(methylbenzylidene)-D-sorbitol (di form) 0.1 Purified water to 100 Dyes, fragrances, preservatives, sequestering agents N-methylpyrrolidone with appropriate amount of mono- and di-isomer dissolved at 60-70°
After adding and dissolving in purified water at step C, other components are added and dissolved.
これを冷却して得られたクリームシャンプーは経時安定
性に優れ、且つ使用感もよかった。The cream shampoo obtained by cooling this was excellent in stability over time and had a good feel on use.
3
(実施例14) O/W乳化口紅
精製水 to 100%
モノベンジリデン−D−ソルビトール(モノ体) 5ジ
ベンジリデン−の−ソルビトール(ジ体)5PLcG−
15003
K O)T □、5
ステアリン酸 z5
セチルアルコール L5
流動パラフィン 8
POKモノオレイン酸エステル 1
顔料 4
肩
防椿剤 適量
香料
精製水にPFtG−1500,KOH、% /体、ジ体
を溶解し、70°Cに保つ(水相)。他の成分を混合し
て7゜°Cに加熱する(油相)。水相に油相を加え均一
に乳化後、容器に流し込み冷却固化した。こうして得ら
れた口紅は内相に油分を含み、外相が水系の全く新規な
タイプの口紅で、ベタっきがなく使用を
性に優れてい÷。3 (Example 14) O/W emulsified lipstick purified water to 100% Monobenzylidene-D-sorbitol (mono form) 5 Dibenzylidene-D-sorbitol (di form) 5PLcG-
15003 K O)T □, 5 Stearic acid z5 Cetyl alcohol L5 Liquid paraffin 8 POK monooleic acid ester 1 Pigment 4 Shoulder prevention agent Dissolve an appropriate amount of PFtG-1500, KOH, % / body, di body in perfume purified water, Keep at 70°C (aqueous phase). Mix other ingredients and heat to 7°C (oil phase). The oil phase was added to the water phase and the mixture was uniformly emulsified, then poured into a container and cooled to solidify. The resulting lipstick is a completely new type of lipstick that contains oil in its inner phase and water-based outer phase, and is non-sticky and easy to use.
4
(実施例15) O/W型乳液
精製水 to 100%
プロピレングリコール 5
モルホリン 2
モノベンジリデン−D−ソルビトール(モノ体) 0.
1ジベンジリデン−D−ソルビトール(ジ体) α9ス
クワラン 3
ステアリン酸 1.5
セチルアルコール 05
ミツロウ 2
POEソルビタンモノオレート 1
グリセリルモノステアリン酸エステル(自己$17[J
) 1香料 適量
防腐剤
プロピレングリコール及びモノ体、ジ体を溶解したモル
ホリンを精製水に加え70°Cに加熱する(水相)。他
の残分を混合して70 ’Cに加熱する(油相)。4 (Example 15) O/W type emulsion purified water to 100% Propylene glycol 5 Morpholine 2 Monobenzylidene-D-sorbitol (mono form) 0.
1 Dibenzylidene-D-sorbitol (di form) α9 Squalane 3 Stearic acid 1.5 Cetyl alcohol 05 Beeswax 2 POE sorbitan monooleate 1 Glyceryl monostearate (self $17 [J
) 1 Fragrance Add an appropriate amount of preservative propylene glycol and morpholine in which mono- and di-forms are dissolved to purified water and heat to 70°C (aqueous phase). Mix other residues and heat to 70'C (oil phase).
水相に油相を加え均一に乳化後、攪拌しながら冷却した
。得られた乳液は従来のものより経時の分へ−
離安定性、使用性が優れてい守。The oil phase was added to the water phase and the mixture was uniformly emulsified, followed by cooling with stirring. The resulting emulsion has better release stability and ease of use over time than conventional ones.
Claims (1)
、(II)式で示される化合物の1種又は2種以上とを
含有することを特徴とする水系化粧料。 HH (1)式 (II)式 C式中、Rは水素原子、カルボキシル基、炭素数1〜3
のアルキル基、アルキル部分の炭素数が1〜3のアルコ
キン基から選ばれた原子又は基を表わし、nは1又は2
の整数を示す。)2、(I)式で示される化合物の1種
又は2種以上と(II)比が90 : 10及至1o
: 90 (重量比)である特許請求の範囲第一項記載
の水系化粧料0 (以下余白)[Claims] 1. An aqueous system containing one or more compounds represented by formula (1) and one or more compounds represented by formula (II) Cosmetics. HH (1) Formula (II) Formula C In the formula, R is a hydrogen atom, a carboxyl group, and a carbon number of 1 to 3
represents an atom or group selected from an alkyl group, an alkoxy group whose alkyl moiety has 1 to 3 carbon atoms, and n is 1 or 2.
indicates an integer. )2, one or more compounds represented by formula (I) and (II) in a ratio of 90:10 to 10
: 90 (weight ratio) of the water-based cosmetic according to claim 1, which is 0 (hereinafter referred to as the margin)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12377083A JPS6016909A (en) | 1983-07-07 | 1983-07-07 | Water-based cosmetic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12377083A JPS6016909A (en) | 1983-07-07 | 1983-07-07 | Water-based cosmetic |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6016909A true JPS6016909A (en) | 1985-01-28 |
Family
ID=14868845
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12377083A Pending JPS6016909A (en) | 1983-07-07 | 1983-07-07 | Water-based cosmetic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6016909A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998023604A1 (en) * | 1996-11-28 | 1998-06-04 | New Japan Chemical Co., Ltd. | Sugar compounds, gelling agents, gelling agent compositions, processes for the preparation of them, and gel compositions |
-
1983
- 1983-07-07 JP JP12377083A patent/JPS6016909A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998023604A1 (en) * | 1996-11-28 | 1998-06-04 | New Japan Chemical Co., Ltd. | Sugar compounds, gelling agents, gelling agent compositions, processes for the preparation of them, and gel compositions |
US6187842B1 (en) | 1996-11-28 | 2001-02-13 | New Japan Chemical Co., Ltd. | Sugar compounds, gelling agents, gelling agent compositions processes for the preparation of them, and gel compositions |
CN1101389C (en) * | 1996-11-28 | 2003-02-12 | 新日本理化株式会社 | Sugar compounds, gelling agents, gelling agent compositions, processes for the preparation of them and gel compositions |
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