JPH1017430A - Irritation-preventing agent, and cosmetic containing the same for preventing irritation - Google Patents
Irritation-preventing agent, and cosmetic containing the same for preventing irritationInfo
- Publication number
- JPH1017430A JPH1017430A JP8190089A JP19008996A JPH1017430A JP H1017430 A JPH1017430 A JP H1017430A JP 8190089 A JP8190089 A JP 8190089A JP 19008996 A JP19008996 A JP 19008996A JP H1017430 A JPH1017430 A JP H1017430A
- Authority
- JP
- Japan
- Prior art keywords
- trehalose
- irritation
- preventing
- cosmetic
- agent
- 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
Landscapes
- Saccharide Compounds (AREA)
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、皮膚、毛髪、爪の
保護に有益な刺激防御剤及びこれを含有する刺激防御用
の化粧料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a stimulant-protecting agent useful for protecting skin, hair and nails and a stimulant-protecting cosmetic containing the same.
【0002】[0002]
【従来の技術】近年に於ける環境の悪化はこれまでの社
会生活では想像だに出来なかった、様々な悪影響を人体
に及ぼしつつある。例えば、オゾン層の破壊は紫外線の
透過量を増大させ、皮膚癌の発生を促進しているし、N
OXやSOXと言った生産活動の副産物や植生の変化に
よって増大した杉などの花粉、人間の生活空間が増大し
たことが原因の一つとなっているダニやほこり等は、皮
膚の炎症や損傷の原因となったり、アトピー性皮膚炎な
どの過剰生体防衛反応発現の引き金になっているとも言
われている。又、これらの紫外線や化学物質は皮膚のみ
ならず毛髪にも悪影響を与えており、切れ毛や枝毛の発
生が近年増加しているとの報告もある。この様な環境変
化に対して、紫外線については、紫外線吸収剤などの開
発により様々な紫外線防護化粧料が開発され対処されて
いるが、上記刺激物質に対しては、炎症や障害によって
損なわれた皮膚機能を保湿剤等によって補完する程度し
か対応策がなかった。即ち、この様な刺激物質による刺
激を、刺激物質の侵入や起炎症作用の発現を防止して、
抑制する手段が求められていた。2. Description of the Related Art The deterioration of the environment in recent years is exerting various adverse effects on the human body which could not be imagined in conventional social life. For example, depletion of the ozone layer increases the transmission of ultraviolet light, promotes the development of skin cancer,
Pollen such as cedar, which has increased due to changes in vegetation and by-products of production activities such as OX and SOX, as well as mites and dust, which are one of the causes of increased human living space, are skin irritation and damage. It is also said to be a cause or trigger of excessive biological defense reactions such as atopic dermatitis. In addition, it has been reported that these ultraviolet rays and chemical substances have an adverse effect not only on the skin but also on the hair, and the occurrence of cut hair and split ends has increased in recent years. In response to such environmental changes, various ultraviolet protective cosmetics have been developed and dealt with with respect to ultraviolet rays by developing ultraviolet absorbers and the like, but the above irritants have been impaired by inflammation and disorders. There were only countermeasures to the extent that skin functions were complemented by moisturizers and the like. That is, the stimulation by such a stimulant is prevented by preventing the intrusion of the stimulus and the manifestation of the inflammatory effect.
There was a need for a means to suppress it.
【0003】一方、トレハロース又はその誘導体から選
ばれる1種乃至は2種以上について、著しい保水作用に
起因する皮膚保護作用は知られていたが、刺激物質に由
来する刺激を抑制する作用は全く知られていなかった。On the other hand, one or more selected from trehalose or a derivative thereof has been known to have a skin-protecting action due to a remarkable water-retaining action, but has no known action to suppress irritation caused by irritants. Had not been.
【0004】[0004]
【発明が解決しようとする課題】本発明はこの様な状況
下行われたものであり、刺激物質に由来する刺激を抑制
する手段を提供することを課題とする。SUMMARY OF THE INVENTION The present invention has been made under such circumstances, and it is an object of the present invention to provide means for suppressing a stimulus derived from a stimulating substance.
【0005】[0005]
【課題を解決するための手段】この様な状況に鑑みて、
本発明者等は刺激物質に由来する刺激に対して、皮膚、
毛髪、爪等の生体各部を保護しうる物質を求めて研究を
重ねた結果、トレハロース又はその誘導体から選ばれる
1種乃至は2種以上にその様な作用を見いだし発明を完
成させた。以下、本発明について詳細に説明する。In view of such a situation,
The present inventors have found that the skin,
As a result of repeated studies on substances capable of protecting various parts of the living body such as hair and nails, one or more kinds of trehalose or its derivatives were found to have such an effect, and the invention was completed. Hereinafter, the present invention will be described in detail.
【0006】[0006]
(1)本発明の刺激防御剤 本発明の刺激防御剤は上記トレハロース又はその誘導体
からなる。トレハロースは復活草中に存在が見いだされ
たもので、著しい保水性を有していることが既に知られ
ている。このものは、既に市販されている。又、その誘
導体としては、例えば、水酸基を硫酸化した硫酸化トレ
ハロース、アシル化したアシル化トレハロース、アルキ
ル化したアルキル化トレハロースが例示でき、これらは
常法に従って誘導化される。又、これらも既に市販され
ており、入手も容易である。これらの内では、硫酸化ト
レハロースが最も好ましい。勿論、このものの生理的に
許容されるこれらの塩も本発明の刺激防御剤に含まれ
る。生理的に許容される塩としては、ナトリウム、カリ
ウム等のアルカリ金属塩、カルシウム、マグネシウム等
のアルカリ土類金属、アンモニウム塩、トリエチルアミ
ンやトリエタノールアミン等の有機アミン塩、リジンや
アルギニン等の塩基性アミノ酸塩等が例示できる。(1) The stimulus-protecting agent of the present invention The stimulating-protective agent of the present invention comprises the above trehalose or a derivative thereof. Trehalose has been found in resurrected grasses and is already known to have significant water retention. It is already commercially available. Examples of the derivatives include sulfated trehalose in which a hydroxyl group is sulfated, acylated acylated trehalose, and alkylated alkylated trehalose, which are derivatized according to a conventional method. Also, these are already commercially available and easily available. Of these, sulfated trehalose is most preferred. Of course, the physiologically acceptable salts thereof are also included in the stimulus-protecting agent of the present invention. Physiologically acceptable salts include alkali metal salts such as sodium and potassium, alkaline earth metals such as calcium and magnesium, ammonium salts, organic amine salts such as triethylamine and triethanolamine, and basic salts such as lysine and arginine. Examples include amino acid salts and the like.
【0007】(2)本発明の刺激防御用の化粧料 本発明の刺激防御用の化粧料は、上記刺激防御剤を含有
することを特徴とする。本発明の刺激防御用の化粧料に
於ける、刺激防御剤の好ましい含有量は、0.001〜
20重量%であり、より好ましくは0.01〜15重量
%であり、更に好ましくは0.05〜10重量%であ
る。本発明の刺激防御化粧料としては、クリーム、乳
液、化粧水などの皮膚用の化粧料、ヘアトニック、ヘア
クリーム、リンス等の毛髪用化粧料、シャンプー、石鹸
等の洗浄料、ネイルカラー等の美爪化粧料、ファンデー
ション、アイカラー、チークカラー、リップカラー等の
メークアップ化粧料、バスバブル等の浴用剤等が挙げら
れる。本発明の刺激防御剤は皮膚化粧料やメークアップ
化粧料や洗浄料や浴用剤に於いては、刺激物質より皮膚
を保護し、毛髪化粧料や洗浄料に於いては、刺激物質よ
り毛髪を保護し、美爪化粧料に於いては黄変の原因とな
ると言われているニトロ化合物より爪を保護することが
出来る。本発明の化粧料に於いては、必須成分である、
刺激防御剤以外に通常化粧料で用いられる任意成分を含
有することが可能である。この様な任意成分としては、
例えば、ワセリンやマイクロクリスタリンワックス等の
ような炭化水素類、ホホバ油やゲイロウ等のエステル
類、牛脂、オリーブ油等のトリグリセライド類、セタノ
ール、オレイルアルコール等の高級アルコール類、ステ
アリン酸、オレイン酸等の脂肪酸、グリセリンや1,3
−ブタンジオール等の多価アルコール類、非イオン界面
活性剤、アニオン界面活性剤、カチオン界面活性剤、両
性界面活性剤、エタノール、カーボポール等の増粘剤、
防腐剤、紫外線吸収剤、抗酸化剤、色素、粉体類等が挙
げられる。かくして得られた本発明の化粧料は、化学物
質、ダニ、埃、花粉等の刺激物質による刺激を抑制する
作用に優れる。(2) Cosmetic for irritation protection of the present invention The cosmetic for irritation protection of the present invention is characterized by containing the above-mentioned irritation protective agent. The preferred content of the stimulant protective agent in the stimulant protective cosmetic of the present invention is 0.001 to 0.001.
It is 20% by weight, more preferably 0.01 to 15% by weight, and still more preferably 0.05 to 10% by weight. Examples of the stimulant protection cosmetics of the present invention include creams, emulsions, skin cosmetics such as lotions, hair tonics, hair creams, hair cosmetics such as rinses, shampoos, soaps and other cleansing agents, nail colors and the like. Examples include make-up cosmetics such as beautiful nail cosmetics, foundations, eye colors, cheek colors, and lip colors, and bath agents such as bath bubbles. The stimulant protective agent of the present invention protects the skin from irritating substances in skin cosmetics, makeup cosmetics, cleansing agents and bath preparations, and protects hair from irritating substances in hair cosmetics and cleaning agents. It can protect and protect nails from nitro compounds, which are said to cause yellowing in beauty nail cosmetics. In the cosmetic of the present invention, is an essential component,
In addition to the stimulant protective agent, it is possible to contain an optional component usually used in cosmetics. Such optional components include:
For example, hydrocarbons such as petrolatum and microcrystalline wax, esters such as jojoba oil and gay wax, triglycerides such as tallow, olive oil, higher alcohols such as cetanol and oleyl alcohol, and fatty acids such as stearic acid and oleic acid. , Glycerin or 1,3
Polyhydric alcohols such as butanediol, nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, ethanol, thickeners such as carbopol,
Examples include preservatives, ultraviolet absorbers, antioxidants, pigments, powders, and the like. The cosmetic of the present invention thus obtained has an excellent action of suppressing irritation caused by irritants such as chemical substances, mites, dust, and pollen.
【0008】[0008]
<実施例1〜4>下記の表1に示す処方に従って化粧水
を作成した。即ち、処方成分を80℃で攪拌し可溶化さ
せ冷却し化粧水を得た。以後、処方の数値は重量部を表
す。<Examples 1 to 4> Lotions were prepared according to the formulations shown in Table 1 below. That is, the ingredients were stirred at 80 ° C. to solubilize and cool to obtain a lotion. Hereinafter, the numerical values of the prescription indicate parts by weight.
【0009】[0009]
【表1】 [Table 1]
【0010】<実施例5〜8>下記の表2に示す処方に
従って化粧水を作成した。即ち、処方成分を80℃で攪
拌し可溶化させ冷却し化粧水を得た。<Examples 5 to 8> Lotions were prepared according to the formulations shown in Table 2 below. That is, the ingredients were stirred at 80 ° C. to solubilize and cool to obtain a lotion.
【0011】[0011]
【表2】 [Table 2]
【0012】<実施例9〜12>下記の表3に示す処方
に従ってクリームを作成した。即ち、イ、ロ、ハをそれ
ぞれ80℃に加熱し、イを混練りし、これをロで希釈
し、このものにハを徐々に加え乳化し、攪拌冷却しクリ
ームを得た。<Examples 9 to 12> Creams were prepared according to the formulations shown in Table 3 below. That is, a, b, and c were each heated to 80 ° C, kneaded with b, diluted with b, gradually added with c, emulsified, stirred and cooled to obtain a cream.
【0013】[0013]
【表3】 [Table 3]
【0014】<実施例13>下記の処方に従ってファン
デーションを作成した。即ち、イ、ロ、ハ、をそれぞれ
80℃で加熱溶解し、イを良く混練りし、これをロで希
釈し、ニを分散し、これにハを徐々に加え乳化し、攪拌
冷却してファンデーションを得た。 イ 硫酸化トレハロースNa 1 マルチトール70%Aq 10シ゛ク゛リセリルモノオレート 5 メチルパラベン 0.3 ロ 流動パラフィン 15マイクロクリスタリンワックス 5 ハ 水 42.7 ニ タルク 7 酸化チタン 10 黄色酸化鉄 3 ベンガラ 1Example 13 A foundation was prepared according to the following formulation. That is, a, b, and c were each heated and dissolved at 80 ° C, kneaded well with b, diluted with b, dispersed in d, gradually added with c, emulsified, and stirred and cooled. Got a foundation. B Sulfated trehalose Na 1 Maltitol 70% Aq 10 Diglyceryl monooleate 5 Methyl paraben 0.3 B Liquid paraffin 15 Microcrystalline wax 5 C Water 42.7 Nitarc 7 Titanium oxide 10 Yellow iron oxide 3 Bengala 1
【0015】<実施例14>下記処方に従ってシャンプ
ーを作成した。即ち、処方成分を加熱溶解し冷却してシ
ャンプーを得た。 椰子油脂肪酸ジエタノールアミド 10 POE(20)ラウリル硫酸ナトリウム 10 1,3−ブタンジオール 5 硫酸化トレハロースNa 1 水 74Example 14 A shampoo was prepared according to the following formulation. That is, the prescription components were dissolved by heating and cooled to obtain a shampoo. Coconut oil fatty acid diethanolamide 10 POE (20) sodium lauryl sulfate 10 1,3-butanediol 5 sulfated trehalose Na 1 water 74
【0016】<実施例15>下記処方に従ってヘアトニ
ックを作成した。即ち、処方成分を加熱溶解し、攪拌冷
却しヘアトニックを得た。 l−メントール 0.1 エチニルエストラジオール 0.1 トウガラシチンキ 0.1 硫酸化トレハロースNa 0.1 1,3−ブタンジオール 5 エタノール 45 水 49.6Example 15 A hair tonic was prepared according to the following formulation. That is, the formulation components were heated and dissolved, and then stirred and cooled to obtain a hair tonic. 1-menthol 0.1 ethinyl estradiol 0.1 pepper tincture 0.1 sulfated trehalose Na 0.1 1,3-butanediol 5 ethanol 45 water 49.6
【0017】<実施例16>下記処方に従って、浴用剤
を作成した。即ち、処方成分をニーダーで混練りし、分
包して浴用剤を得た。 炭酸ナトリウム 40 硫酸ナトリウム 50 トレハロース 10Example 16 A bath agent was prepared according to the following formulation. That is, the prescription components were kneaded with a kneader and divided to obtain a bath agent. Sodium carbonate 40 sodium sulfate 50 trehalose 10
【0018】<実施例17>実施例1〜12の化粧料に
ついて、ICRマウス1群10匹(雄性、体重20〜3
0g)を用いて、刺激防御作用の検討を行った。即ち、
背部を剃毛し化粧料を0.05ml投与し、更にラウリ
ル硫酸ナトリウムの1%水溶液を0.05ml24時間
クローズドパッチした。この作業を4回繰り返し、最後
のパッチ除去後72時間に皮膚の鱗屑、紅斑、コンダク
タンスについて測定した。鱗屑と紅斑は非常に強いを2
点、明かを1点、微弱を0.5点として評点をつけた。
コンダクタンス(μΩ-1)はコルネオメーターによって
測定した。平均評点とコンダクタンスを表4に示す。対
照1としては、実施例1の硫酸化トレハロースナトリウ
ムを水に置き換えたもの、対照2としては実施例9の酢
酸化トレハロースを水に置き換えたものを用い、比較例
1としては、実施例1の硫酸化トレハロースナトリウム
を保湿作用などの従来の肌保護機能を有することが知ら
れている、レシチンに置き換えたものを、比較例2とし
ては実施例9の酢酸化トレハロースを同じくレシチンに
置き換えたものを用いた。本発明の刺激防御剤は刺激物
質の刺激から生体を保護する作用に優れることが判る。
この作用は物理的接触を妨害することにより刺激物質と
の接触やその侵入を防いでいることのみに由来しないこ
と、即ち、本発明の刺激防護剤が刺激発現そのものを抑
制していることは、比較例1及び2との比較より明かで
ある。Example 17 The cosmetics of Examples 1 to 12 were used for a group of 10 ICR mice (male, body weight 20 to 3).
0g) was used to examine the stimulus-protective effect. That is,
The back was shaved, 0.05 ml of cosmetic was administered, and 0.05 ml of a 1% aqueous solution of sodium lauryl sulfate was subjected to closed patching for 24 hours. This operation was repeated four times, and the scale, erythema, and conductance of the skin were measured 72 hours after the last patch was removed. Scale and erythema are very strong 2
The score was given as 1 point for the point and the clear, and 0.5 point for the weak.
The conductance (μΩ -1 ) was measured by a corneometer. Table 4 shows the average score and conductance. Control 1 was obtained by replacing sodium sulfated trehalose of Example 1 with water, Control 2 was obtained by replacing acetic acid trehalose of Example 9 by water, and Comparative Example 1 was obtained by using Example 1 What replaced sodium sulfated trehalose with lecithin, which is known to have a conventional skin protection function such as moisturizing action, as Comparative Example 2 was obtained by replacing the acetated trehalose of Example 9 with lecithin. Using. It can be seen that the stimulus-protecting agent of the present invention is excellent in protecting the living body from stimulus of stimulating substances.
This effect does not stem only from preventing contact with or invasion of stimulants by interfering with physical contact, that is, the fact that the stimulant protective agent of the present invention suppresses stimulus expression itself means that It is clear from the comparison with Comparative Examples 1 and 2.
【0019】[0019]
【表4】 [Table 4]
【0020】[0020]
【発明の効果】本発明によれば、刺激物質に由来する刺
激を抑制する手段を提供できる。According to the present invention, it is possible to provide a means for suppressing a stimulus derived from a stimulating substance.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A61K 7/40 A61K 7/40 7/48 7/48 7/50 7/50 C07H 3/04 C07H 3/04 13/00 13/00 13/06 13/06 15/04 15/04 A ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification number Agency reference number FI Technical display location A61K 7/40 A61K 7/40 7/48 7/48 7/50 7/50 C07H 3/04 C07H 3/04 13/00 13/00 13/06 13/06 15/04 15/04 A
Claims (8)
激防御剤。1. A stimulant protective agent comprising trehalose or a derivative thereof.
ース又はアシル化トレハロースである、請求項1記載の
刺激防護剤。2. The stimulant protective agent according to claim 1, wherein the derivative of trehalose is sulfated trehalose or acylated trehalose.
ばれる1種乃至は2種以上を含有する刺激防護用の化粧
料。3. A stimulus-protecting cosmetic comprising one or more selected from the stimulant-protecting agents according to claim 1.
量が0.001〜20重量%である、請求項3記載の化
粧料。4. The cosmetic according to claim 3, wherein the content of the stimulant protective agent according to claim 1 or 2 is 0.001 to 20% by weight.
ある、請求項3又は4記載の化粧料。5. The cosmetic according to claim 3, wherein the use is for skin protection, hair protection or nail protection.
る1種乃至は2種以上を含有する刺激防護用の化粧料。6. A stimulant-protecting cosmetic containing one or more selected from trehalose or a derivative thereof.
ース又はアシル化トレハロースである、請求項6記載の
化粧料。7. The cosmetic according to claim 6, wherein the trehalose derivative is sulfated trehalose or acylated trehalose.
る1種乃至は2種以上の含有量が0.001〜20重量
%である、請求項6又は7記載の化粧料。8. The cosmetic according to claim 6, wherein the content of one or more selected from trehalose or a derivative thereof is 0.001 to 20% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8190089A JPH1017430A (en) | 1996-07-01 | 1996-07-01 | Irritation-preventing agent, and cosmetic containing the same for preventing irritation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8190089A JPH1017430A (en) | 1996-07-01 | 1996-07-01 | Irritation-preventing agent, and cosmetic containing the same for preventing irritation |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH1017430A true JPH1017430A (en) | 1998-01-20 |
Family
ID=16252190
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8190089A Pending JPH1017430A (en) | 1996-07-01 | 1996-07-01 | Irritation-preventing agent, and cosmetic containing the same for preventing irritation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH1017430A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH1045560A (en) * | 1996-08-06 | 1998-02-17 | Kanebo Ltd | Skin mucous membrane-stimulation emollient |
JPH10306011A (en) * | 1997-05-07 | 1998-11-17 | Pola Chem Ind Inc | Ununiformity improving cosmetic |
JPH11255617A (en) * | 1998-03-10 | 1999-09-21 | Pola Chem Ind Inc | Makeup cosmetic for improving skin condition |
JP2001002552A (en) * | 1999-06-23 | 2001-01-09 | Pola Chem Ind Inc | Skin protective cosmetic |
JP2002363060A (en) * | 2001-06-06 | 2002-12-18 | Kanebo Ltd | Bathing agent |
JP2003034612A (en) * | 2000-09-28 | 2003-02-07 | Hiromaito Co Ltd | Composition for percutaneous absorption of carbon dioxide and use and usage thereof |
JP2004107233A (en) * | 2002-09-17 | 2004-04-08 | Kuraray Co Ltd | Skin care preparation for external use |
US6800302B2 (en) | 2001-03-30 | 2004-10-05 | L'oreal S.A. | Heat activated durable styling compositions comprising C1 to C22 Substituted C3-C5 monosaccharides and methods for same |
JP2007269692A (en) * | 2006-03-31 | 2007-10-18 | Pola Chem Ind Inc | Cosmetic material for softening skin |
JP2019508459A (en) * | 2016-03-18 | 2019-03-28 | ユニリーバー・ナームローゼ・ベンノートシヤープ | Hair treatment composition |
-
1996
- 1996-07-01 JP JP8190089A patent/JPH1017430A/en active Pending
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH1045560A (en) * | 1996-08-06 | 1998-02-17 | Kanebo Ltd | Skin mucous membrane-stimulation emollient |
JPH10306011A (en) * | 1997-05-07 | 1998-11-17 | Pola Chem Ind Inc | Ununiformity improving cosmetic |
JPH11255617A (en) * | 1998-03-10 | 1999-09-21 | Pola Chem Ind Inc | Makeup cosmetic for improving skin condition |
JP2001002552A (en) * | 1999-06-23 | 2001-01-09 | Pola Chem Ind Inc | Skin protective cosmetic |
JP2003034612A (en) * | 2000-09-28 | 2003-02-07 | Hiromaito Co Ltd | Composition for percutaneous absorption of carbon dioxide and use and usage thereof |
US6800302B2 (en) | 2001-03-30 | 2004-10-05 | L'oreal S.A. | Heat activated durable styling compositions comprising C1 to C22 Substituted C3-C5 monosaccharides and methods for same |
JP2002363060A (en) * | 2001-06-06 | 2002-12-18 | Kanebo Ltd | Bathing agent |
JP4582960B2 (en) * | 2001-06-06 | 2010-11-17 | 塩水港精糖株式会社 | Bath composition |
JP2004107233A (en) * | 2002-09-17 | 2004-04-08 | Kuraray Co Ltd | Skin care preparation for external use |
JP2007269692A (en) * | 2006-03-31 | 2007-10-18 | Pola Chem Ind Inc | Cosmetic material for softening skin |
JP2019508459A (en) * | 2016-03-18 | 2019-03-28 | ユニリーバー・ナームローゼ・ベンノートシヤープ | Hair treatment composition |
US11369555B2 (en) | 2016-03-18 | 2022-06-28 | Conopco, Inc. | Hair treatment compositions |
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