JPH0436227A - Hair cosmetic - Google Patents

Hair cosmetic

Info

Publication number
JPH0436227A
JPH0436227A JP14403090A JP14403090A JPH0436227A JP H0436227 A JPH0436227 A JP H0436227A JP 14403090 A JP14403090 A JP 14403090A JP 14403090 A JP14403090 A JP 14403090A JP H0436227 A JPH0436227 A JP H0436227A
Authority
JP
Japan
Prior art keywords
hair
cosmetic
resins
resin
nonionic surfactant
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.)
Granted
Application number
JP14403090A
Other languages
Japanese (ja)
Other versions
JPH0613450B2 (en
Inventor
Masaki Kinami
木浪 正樹
Akio Maekawa
前川 明男
Masaya Yasuno
保野 昌也
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sunstar Inc
Original Assignee
Sunstar Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sunstar Inc filed Critical Sunstar Inc
Priority to JP2144030A priority Critical patent/JPH0613450B2/en
Publication of JPH0436227A publication Critical patent/JPH0436227A/en
Publication of JPH0613450B2 publication Critical patent/JPH0613450B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Cosmetics (AREA)

Abstract

PURPOSE:To provide the title cosmetic highly safe to the skin, having excellent hair trimming ability, capable of forming a transparent, highly rinsable resin film and of giving polish to the hair, formulated with a hair-setting resin and pyroglutamic ester-based nonionic surfactant. CONSTITUTION:The objective cosmetic can be obtained by incorporation of (A) 1-5wt.%, on a solid basis, of at least one kind of hair-setting resin selected from amphoteric resins, anionic resins, cationic resins, nonionic resins, etc., (B) 0.03-0.50wt.% of a nonionic surfactant (e.g. polyoxyethylene glyceryl pyroglutamic-isostearic diester), and approximately (C) such ingredients as plasticizer, antioxidant, ultraviolet light absorber and/or perfume, followed by preparation through a conventional method, thus obtaining the objective cosmetic. The present cosmetic can be prepared in the form of hair mist, hair spray etc.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は頭髪用化粧料、特に皮膚に対する安全性が高く
、優れた整髪力を有しかつ透明で洗い落ちのよい樹脂膜
を形成し頭髪に優れた艶を与える頭髪用化粧料に関する
Detailed Description of the Invention [Industrial Field of Application] The present invention provides hair cosmetics, particularly those that are highly safe for the skin, have excellent hair styling ability, and form a transparent resin film that is easy to wash off. This invention relates to a hair cosmetic that gives excellent shine to hair.

[従来の技術及び課題] 従来、毛髪を固定しヘアスタイルを整えるヘアミスト、
ヘアスプレーなどの頭髪用(整髪)化粧料には、主に香
料及び油分を可溶化するため各種の界面活性剤が配合さ
れている。しかしながら、このような界面活性剤は、整
髪力を付与するために配合された毛髪固定用樹脂の皮膜
透明性を損い、毛髪のツヤを低下させる。また、従来の
頭髪用化粧料に配合されているカチオン系、ノニオン系
の界面活性剤は皮膚に対する安全性が充分ではない。
[Conventional techniques and issues] Conventionally, hair mist that fixes hair and adjusts hair style;
BACKGROUND ART Hair (hair styling) cosmetics such as hair sprays contain various surfactants mainly to solubilize fragrances and oils. However, such surfactants impair the transparency of the film of the hair fixing resin blended to impart hair styling ability, and reduce the shine of the hair. Furthermore, cationic and nonionic surfactants that are blended into conventional hair cosmetics are not sufficiently safe for the skin.

本発明者らは、かかる観点から安全性が高く毛髪へのな
じみのよいアミノ酸系活性剤を頭髪用化粧料に配合する
ことを検討した。その結果、毛髪固定用樹脂に組み合わ
せる界面活性剤としてアミノ酸系界面活性剤のうちでも
、特にピログルタミン酸エステル系非イオン界面活性剤
を選択することにより皮膚に対する安全性と共に良好な
透明性、洗い落ち性を何する樹脂被膜が得られ優れた毛
髪の艶かもたらされることを見いだし本発明を完成する
に至った。
From this point of view, the present inventors have investigated incorporating into hair cosmetics an amino acid-based active agent that is highly safe and blends well with the hair. As a result, by selecting a pyroglutamic acid ester nonionic surfactant among amino acid surfactants as a surfactant to be combined with the hair fixing resin, we have achieved safety for the skin as well as good transparency and washability. The present inventors have discovered that a resin coating can be obtained that provides excellent hair luster, and has completed the present invention.

従来より、グルタミン酸エステル系の界面活性剤を皮膚
や頭髪に温和な界面活性剤としてリンス、ンヤンブーな
ど一部の頭髪用化粧料に配合することは知られている。
BACKGROUND ART It has been known that glutamate ester-based surfactants are incorporated into some hair cosmetics, such as rinses and Nyanbu, as surfactants that are mild to the skin and hair.

しかしながら、整髪用化粧料において毛髪表面に被膜を
形成する毛髪固定用樹脂との組み合わせについて検討さ
れたものはない。
However, no hair styling cosmetics have been studied in combination with hair fixing resins that form a film on the hair surface.

[課題を解決するための手段] 本発明は、毛髪固定用樹脂およびピログルタミン酸エス
テル系の非イオン界面活性剤を配合した頭髪用化粧料を
提供するものである。
[Means for Solving the Problems] The present invention provides a hair cosmetic containing a hair fixing resin and a pyroglutamic acid ester nonionic surfactant.

本発明の頭髪化粧料に配合される毛髪固定用樹脂として
は、両性樹脂、アニオン樹脂、カチオン樹脂、ノニオン
樹脂などが挙げられる。
Examples of the hair fixing resin to be incorporated into the hair cosmetic of the present invention include amphoteric resins, anionic resins, cationic resins, and nonionic resins.

両性樹脂としては、ジアルキルアミノエチルメタクリレ
ート重合物のモノクロル酢酸両性化物(ユカフォーマー
AM75、三菱油化型)、オクチルアクリルアミド/ブ
チルアミノメチルメタクリレート/アクリル酸/アクリ
ル酸エステル重合物(八MPtlOMER,NSC製)
などが挙げられる。
Examples of amphoteric resins include monochloroacetic acid ampholyte of dialkylaminoethyl methacrylate polymer (Yukaformer AM75, Mitsubishi Yuka type), octylacrylamide/butylaminomethyl methacrylate/acrylic acid/acrylic acid ester polymer (8MPtlOMER, manufactured by NSC)
Examples include.

アニオン樹脂としては、アクリル酸エステル/メタアク
リル酸エステル共重合物(プラスサイズ互応化学製)、
酢酸ビニル/クロトン酸共重合物(レジン2B−131
0,NSC製)、酢酸ビニル/クロトン酸/ビニルネオ
デカネート共重合物(レジン28−2930.NSC製
)、メチルビニルエーテルマレイン酸ハーフエステル共
重合物(ガントレッツES、GAF製)などが挙げられ
る。
Examples of anion resins include acrylic ester/methacrylic ester copolymer (manufactured by Plus Size Goo Kagaku),
Vinyl acetate/crotonic acid copolymer (Resin 2B-131
0, manufactured by NSC), vinyl acetate/crotonic acid/vinyl neodecanate copolymer (Resin 28-2930. manufactured by NSC), and methyl vinyl ether maleic acid half ester copolymer (Gantretz ES, manufactured by GAF).

カチオン樹脂として、ジメチルジアリルアンモニウムク
ロライド重合物(Merguat  Ca1gon製)
、ヒドロキシエチルセルロース/ジメチルジアリルアン
モニウムクロライド共重合物(セルコート。
As a cationic resin, dimethyldiallylammonium chloride polymer (manufactured by Merguat Calgon)
, hydroxyethylcellulose/dimethyldiallylammonium chloride copolymer (Celcoat).

NSC製)、ビニルピロリドン四級化ジアルキルアミノ
アルキル(メタ)アクリレート重合体(ガフコート、G
AP製)があげられる。
(manufactured by NSC), vinylpyrrolidone quaternized dialkylaminoalkyl (meth)acrylate polymer (Gaffcoat, G
(manufactured by AP).

ノニオン樹脂として、ポリビニルピロリドン(P■P、
GAF製)、ビニルピロリドン/酢酸ビニル共重合体(
ルビスコールVA、BASFtJ)があげられる。これ
らのうち、頭髪のセット力の点からアニオン樹脂か特に
好ましい。
As a nonionic resin, polyvinylpyrrolidone (P■P,
manufactured by GAF), vinylpyrrolidone/vinyl acetate copolymer (
Rubiscoll VA, BASFtJ). Among these, anionic resins are particularly preferred from the viewpoint of hair setting power.

これら毛髪固定樹脂は、そのINまたは2M以上を化粧
料中固形分として1〜5重櫃%配合するのが好ましい。
It is preferable that IN or 2M or more of these hair fixing resins be blended in the cosmetic composition in an amount of 1 to 5 weight percent as a solid content.

毛髪固定用樹脂の配合量か1重量%未満であると、毛髪
固定用化粧料として十分なセット力が得られない。また
、配合量が5重量%を越えると噴霧機構に詰まり、液ダ
レ等が発生したり、セット剤の霧性状が低下して毛髪に
均一に噴霧できず、毛髪固定用化粧料としての商品価値
か著しく低下する。
If the blending amount of the hair fixing resin is less than 1% by weight, sufficient setting power will not be obtained as a hair fixing cosmetic. In addition, if the blending amount exceeds 5% by weight, the spray mechanism may become clogged, resulting in liquid dripping, or the mist properties of the setting agent may deteriorate, making it impossible to spray the hair uniformly, reducing the commercial value of the hair fixing cosmetic. or decrease significantly.

なお、アニオン性樹脂を用いる場合には、アニオン性の
官能基の一部または全部を2−アミノ2−メチル−1−
プロパツール、トリエタノールアミン等の中和剤で中和
するのがよい。
In addition, when using an anionic resin, some or all of the anionic functional groups are replaced with 2-amino 2-methyl-1-
It is best to neutralize with a neutralizing agent such as propatool or triethanolamine.

つぎに本発明化粧料に配合されるピログルタミン酸エス
テル系の非イオン界面活性剤としては、ポリオキシアル
キレン多価アルコールとピログルタミン酸のエステル、
ポリオキンアルキレン多価アルコールとピログルタミン
酸、脂肪酸のジエステルがあげられる。多価アルコール
としてはグリセリン、ヒマシ油、硬化ヒマシ油、プロピ
レングリコール、エチレングリコール、ノグリセリン等
が、また脂肪酸としてはイソステアリン酸、ミリスチン
酸、ラウリン酸、オレイン酸等があげられる。これらの
ピログルタミン系エステルのうち下CFI−OCOC,
7FI3.(OCR,CH,)。0COC,、H3゜[
式中、R+)) 4 cは20−70である。]で表さ
れるPOE付加硬化ヒマン油ピログルタミン酸イソステ
アリン酸ジエステル(ピロチルCP1、日本エマルノヨ
ン製)および下式[■]。
Next, the pyroglutamic acid ester nonionic surfactants to be incorporated into the cosmetics of the present invention include esters of polyoxyalkylene polyhydric alcohol and pyroglutamic acid,
Examples include diesters of polyoquine alkylene polyhydric alcohols, pyroglutamic acid, and fatty acids. Examples of polyhydric alcohols include glycerin, castor oil, hydrogenated castor oil, propylene glycol, ethylene glycol, noglycerin, etc., and examples of fatty acids include isostearic acid, myristic acid, lauric acid, and oleic acid. Among these pyroglutamine-based esters, CFI-OCOC,
7FI3. (OCR, CH,). 0COC,,H3゜[
In the formula, R+))4c is 20-70. ] and the following formula [■]:

C)l 、 −C)I 。C) l, -C) I.

■ C1−(OCH,CH,)cOCOC,、Has[式中
、λ+b+cは20〜30である。コで表されるPOE
付加グリセリルピログルタミン酸イソステアリン酸ジエ
ステル(ピロチルGP■1日本エマルジョン製)が特に
好ましい。
(2) C1-(OCH, CH,)cOCOC,, Has [where λ+b+c is 20-30. POE represented by
Added glyceryl pyroglutamic acid isostearic acid diester (Pyrothyl GP ■1 manufactured by Nippon Emulsion) is particularly preferred.

これらピログルタミン酸エステルは、そのIIまたは2
種以上を頭髪化粧料中0.03〜0.50重量%配合す
るのが好ましい。ピログルタミン酸エステルの配合量が
0.03重量%未満であると香料の可溶化力が低下し、
低温でオリを生じやすくなる。また、配合量が0.50
重量%を越えると樹脂膜が可塑化され、ベタつきが生じ
る。
These pyroglutamic acid esters are II or 2
It is preferable to incorporate 0.03 to 0.50% by weight of these seeds into the hair cosmetic. If the amount of pyroglutamic acid ester is less than 0.03% by weight, the solubilizing power of the fragrance will decrease,
It is more likely to cause sagging at low temperatures. Also, the blending amount is 0.50
If the amount exceeds % by weight, the resin film becomes plasticized and becomes sticky.

本発明の頭髪用化粧品は、公知の方法によりヘアミスト
、ヘアースプレーなどの形態の各種頭髪用化粧料に調製
される。本発明の頭髪用化粧料には、その性能を損なわ
ない範囲でさらに必要に応じて可塑剤、酸化防止剤、防
腐剤、紫外線吸収剤、植物抽出物、香料等を適宜配合し
てよい。可塑剤としてはプロピレングリコール、ポリプ
ロピレングリコール、グリセリンのようなアルコール類
、ミリスチン酸イソプロピル、ラウリル酸ヘキシル、ミ
リスチン酸オクチルドデシル等のエステル類、ジメチル
ポリシロキサン、メチルフェニルポリシロキサンのよう
なシリコン誘導体があげられる。
The hair cosmetic of the present invention can be prepared into various hair cosmetics in the form of hair mist, hair spray, etc. by known methods. The hair cosmetic of the present invention may further contain plasticizers, antioxidants, preservatives, ultraviolet absorbers, plant extracts, fragrances, etc., as necessary, within a range that does not impair its performance. Examples of plasticizers include alcohols such as propylene glycol, polypropylene glycol, and glycerin, esters such as isopropyl myristate, hexyl laurate, and octyldodecyl myristate, and silicone derivatives such as dimethylpolysiloxane and methylphenylpolysiloxane. .

これらの成分を溶解するにはエタノール、水、エタノー
ル/水混合物、イソプロピルアルコールなどの溶剤が用
いられる。
Solvents such as ethanol, water, ethanol/water mixtures, isopropyl alcohol, etc. are used to dissolve these components.

[実施例コ つぎに本発明を実施例によりさらに具体的に説明する。[Example code] Next, the present invention will be explained in more detail with reference to Examples.

実施例、比較例において配合量は総て重量%である。In Examples and Comparative Examples, all amounts are expressed in weight %.

実施例1(ヘアミスト) 成  分         配合量 コカフオーマー5M75R205S  13.00(3
0%エタノール液) ピロチルCPI−400,10 ポリエチレングリコール      0.lO香料  
             0.10エタノール   
         86.70常法に従い、上記組成に
てヘアミストを調製した。
Example 1 (hair mist) Ingredients Amount Cocaformer 5M75R205S 13.00 (3
0% ethanol solution) Pyrotyl CPI-400,10 Polyethylene glycol 0. lO fragrance
0.10 ethanol
86.70 A hair mist having the above composition was prepared according to a conventional method.

実施例2 成     分           配合量へアース
プレイ プラスサイズL−53PB      8 00(50
%エタノール液) ピロチルGPI−25005 ポリエチレングリコール      OIOプロピレン
グリコール       002香料        
       010エタノール          
  41.73液化石油ガス          50
00常法に従い上記成分を配合して耐圧容器の充填しヘ
アスプレーを調製した。
Example 2 Ingredients Blend amount Earthplay Plus Size L-53PB 800 (50
% ethanol solution) Pyrothyl GPI-25005 Polyethylene glycol OIO Propylene glycol 002 Fragrance
010 ethanol
41.73 Liquefied petroleum gas 50
A hair spray was prepared by blending the above ingredients and filling a pressure container according to a conventional method.

実施例3〜7および比較例1〜8 後記第1表に示す組成にて公知の方法によりヘアースプ
レィを調製し、下記の各項目について評価を行った。す
なわち、アミノ酸系界面活性剤の種類、その配合量の異
なる化粧料を調製し、これを用いて皮膜の透明性、ベタ
つき、洗い落ち、低温安定性を下記の方法により評価し
た。
Examples 3 to 7 and Comparative Examples 1 to 8 Hair sprays were prepared by a known method using the compositions shown in Table 1 below, and the following items were evaluated. That is, cosmetics containing different types and amounts of amino acid surfactants were prepared, and the transparency, stickiness, wash-off, and low-temperature stability of the films were evaluated using the following methods.

(皮膜の透明性) ガラス板に内容物を噴霧し、皮膜が乾燥するまで観察を
行った。
(Transparency of film) The contents were sprayed onto a glass plate, and the film was observed until it dried.

判定基準  O透明 △ 乾燥中に白濁 × 観察中ずっと白濁 (へ夕つき) ガラス板に内容物を噴霧し、10分間乾燥させた後、専
門パネラ−が指で評価した。
Judgment Criteria: O Transparent △ Cloudy during drying × Cloudy throughout observation (cloudy) After spraying the contents onto a glass plate and drying for 10 minutes, an expert panelist evaluated with their fingers.

判定基準  ○ ベタつかない へ ややベタつく X ベタつく (洗い落ち) ガラス板に内容物を噴霧し、10分間乾燥させた後、5
mCの水をかけ、皮膜のとれ具合を観察した。
Judgment criteria ○ Not sticky Slightly sticky
Water of mC was poured on the film and the degree of removal of the film was observed.

判定基準、 ○ 透明に溶解 △ 膨潤しながら溶解 × 溶解しない (低温安定性) 内容物を一5℃の恒温室に24時間放置した後、目視で
判断した。
Judgment criteria: ○ Transparently dissolved △ Dissolved while swelling × Not dissolved (low-temperature stability) Judgment was made visually after the contents were left in a constant temperature room at -5° C. for 24 hours.

判定基準二 〇 透明 × 沈澱 (総合評価) O:4項目すべてが○の場合 へ:1項目でも△があった場合 ×:1項目でもXがあった場合 これらの結果を第1表にあわせ示す。Judgment Criteria 20 Transparent × Precipitation (comprehensive evaluation) O: If all 4 items are ○ To: If even one item is △ ×: If there is an X in even one item These results are also shown in Table 1.

第1表より明らかなように、ピログルタミン酸エステル
を003〜0.05重量%と毛髪固定用樹脂とを配合し
た場合、安定で皮膜の透明性、洗い落ちに優れた頭髪用
化粧品が得られる。
As is clear from Table 1, when 0.03 to 0.05% by weight of pyroglutamic acid ester is blended with a hair fixing resin, a hair cosmetic that is stable, has excellent film transparency, and is easy to wash off can be obtained.

[発明の効果] 本発明の頭髪用化粧料は、良好な整髪力を有しかつ優れ
た透明性と洗い落ちの良い被覆を形成して毛髪にツヤを
与える。また、皮膚に対して高い安全性を有する。
[Effects of the Invention] The hair cosmetic of the present invention has good hair styling ability, forms a coating with excellent transparency and washes off easily, and gives shine to the hair. It also has high safety to the skin.

Claims (4)

【特許請求の範囲】[Claims] (1)毛髪固定用樹脂およびピログルタミン酸エステル
系の非イオン界面活性剤を配合した頭髪用化粧料。
(1) A hair cosmetic containing a hair fixing resin and a pyroglutamic acid ester nonionic surfactant.
(2)毛髪固定用樹脂がアニオン樹脂である前記請求項
1記載の頭髪用化粧料。
(2) The hair cosmetic according to claim 1, wherein the hair fixing resin is an anionic resin.
(3)アニオン樹脂がメチルビニルエーテル・マレイン
酸ハーフエステル共重合体である前記請求項2記載の頭
髪用化粧料。
(3) The hair cosmetic according to claim 2, wherein the anionic resin is a methyl vinyl ether/maleic acid half ester copolymer.
(4)非イオン界面活性剤がポリオキシエチレングリセ
リルピログルタミン酸イソステアリン酸ジエステルであ
る前記請求項1、2または3に記載の頭髪用化粧料。
(4) The hair cosmetic according to claim 1, 2 or 3, wherein the nonionic surfactant is polyoxyethylene glyceryl pyroglutamic acid isostearic acid diester.
JP2144030A 1990-05-31 1990-05-31 Cosmetics for hair Expired - Fee Related JPH0613450B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2144030A JPH0613450B2 (en) 1990-05-31 1990-05-31 Cosmetics for hair

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2144030A JPH0613450B2 (en) 1990-05-31 1990-05-31 Cosmetics for hair

Publications (2)

Publication Number Publication Date
JPH0436227A true JPH0436227A (en) 1992-02-06
JPH0613450B2 JPH0613450B2 (en) 1994-02-23

Family

ID=15352697

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2144030A Expired - Fee Related JPH0613450B2 (en) 1990-05-31 1990-05-31 Cosmetics for hair

Country Status (1)

Country Link
JP (1) JPH0613450B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7781391B2 (en) * 2006-03-17 2010-08-24 Croda, Inc. Amine/amide-functionalized lipophiles
JP2012001464A (en) * 2010-06-15 2012-01-05 Daizo:Kk Undiluted solution for hair spray, and pump product and aerosol product charged with the undiluted solution for hair spray

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5750827A (en) * 1980-09-12 1982-03-25 Lion Corp Hair cosmetics
JPS5758608A (en) * 1980-09-25 1982-04-08 Lion Corp Hairdressing
JPS5758607A (en) * 1980-09-25 1982-04-08 Lion Corp Hairdressing
JPS60126213A (en) * 1983-12-09 1985-07-05 Lion Corp Transparent hair cosmetic composition

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5750827A (en) * 1980-09-12 1982-03-25 Lion Corp Hair cosmetics
JPS5758608A (en) * 1980-09-25 1982-04-08 Lion Corp Hairdressing
JPS5758607A (en) * 1980-09-25 1982-04-08 Lion Corp Hairdressing
JPS60126213A (en) * 1983-12-09 1985-07-05 Lion Corp Transparent hair cosmetic composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7781391B2 (en) * 2006-03-17 2010-08-24 Croda, Inc. Amine/amide-functionalized lipophiles
JP2012001464A (en) * 2010-06-15 2012-01-05 Daizo:Kk Undiluted solution for hair spray, and pump product and aerosol product charged with the undiluted solution for hair spray

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