JP2005179326A - Cosmetic - Google Patents
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- JP2005179326A JP2005179326A JP2003436491A JP2003436491A JP2005179326A JP 2005179326 A JP2005179326 A JP 2005179326A JP 2003436491 A JP2003436491 A JP 2003436491A JP 2003436491 A JP2003436491 A JP 2003436491A JP 2005179326 A JP2005179326 A JP 2005179326A
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Abstract
Description
本発明は、ビタミンC又はビタミンC誘導体を主成分として配合した化粧料に関するものである。 The present invention relates to a cosmetic containing vitamin C or a vitamin C derivative as a main component.
皮膚のシミは、一般的に日光の紫外線によりメラノサイトが活性化されて、その結果、メラノサイトにて合成されたメラニン色素が皮膚内に異常沈着することにより発生する。このようなシミに対して、古くからビタミンC又はビタミンC誘導体が使用されている。 Skin spots generally occur when melanocytes are activated by ultraviolet rays of sunlight, and as a result, melanin pigments synthesized in melanocytes are abnormally deposited in the skin. For such stains, vitamin C or vitamin C derivatives have been used for a long time.
しかし、市販されているビタミンC又はビタミンC誘導体を主成分とした製品は、べたつきを生じる欠点があった。このべたつきを無くすために種々の検討がなされているが、満足のいく製品は市販されていないのが現状である。 However, commercially available products based on vitamin C or vitamin C derivatives have the drawback of causing stickiness. Various studies have been made to eliminate this stickiness, but no satisfactory product is commercially available.
しかしながら、使用者にとって、美白効果があり、安全性の高いビタミンC又はビタミンC誘導体を主成分とし、且つ、使用感がべたつかない製品が望まれている。 However, a product that has a whitening effect, a highly safe vitamin C or a vitamin C derivative as a main component, and a non-sticky feeling is desired for the user.
そこで、本発明者らは、上記の事情を鑑み鋭意研究した結果、特定の原料を配合することにより、べたつき感を抑えた美白効果の高い化粧料が得られることを見出し、本発明に至った。 Thus, as a result of intensive studies in view of the above circumstances, the present inventors have found that a cosmetic material with a high whitening effect with a reduced stickiness can be obtained by blending specific raw materials, resulting in the present invention. .
即ち、本発明は、ビタミンC又はビタミンC誘導体を主成分とし、他の成分2−メタクリロイルオキシエチルホスホリルコリンと疎水性モノマーとの共重合体及び大豆を発酵処理することで得られた高粘性たんぱく質水溶液、更には、ツボクサエキスとの組み合わせにより、ビタミンC又はビタミンC誘導体を主成分としたべたつきを抑えた化粧料を完成した。 That is, the present invention is a highly viscous aqueous protein solution obtained by fermenting soybean and a copolymer of the other component 2-methacryloyloxyethyl phosphorylcholine and a hydrophobic monomer, the main component of which is vitamin C or vitamin C derivative. Furthermore, a combination of vitamin C or a vitamin C derivative as a main component and a reduction in stickiness was completed by a combination with a camellia extract.
本発明の化粧料によれば、ビタミンC又はビタミンC誘導体を主成分として配合することによる、べたつきを抑えた化粧料を得ることができる。 According to the cosmetic of the present invention, it is possible to obtain a cosmetic with reduced stickiness by blending vitamin C or a vitamin C derivative as a main component.
以下、本発明の実施例について詳細に説明する。
本発明に用いるビタミンC又はビタミンC誘導体としては、L−アスコルビン酸及びその誘導体であり、L−アスコルビン酸、L−アスコルビン酸金属塩、L−アスコルビン酸リン酸エステル金属塩、L−アスコルビン酸硫酸エステル金属塩等が挙げられる。又、L−アスコルビン酸2−グルコシド等のL−アスコルビン酸−グルコシド等が挙げられる。金属塩としては、それぞれのNa、K、Mg、Ca、Al塩が挙げられる。Examples of the present invention will be described in detail below.
Vitamin C or vitamin C derivatives used in the present invention are L-ascorbic acid and its derivatives, L-ascorbic acid, L-ascorbic acid metal salt, L-ascorbic acid phosphate metal salt, L-ascorbic acid sulfate Examples thereof include ester metal salts. Moreover, L-ascorbic acid-glucosides, such as L-ascorbic acid 2-glucoside, are mentioned. As a metal salt, each Na, K, Mg, Ca, Al salt is mentioned.
ビタミンC又はビタミンC誘導体の配合量としては、化粧料全量中0.1質量%〜10質量%であり、さらに好ましくは、0.5質量%〜5質量%である。 As a compounding quantity of vitamin C or a vitamin C derivative, it is 0.1 mass%-10 mass% in cosmetics whole quantity, More preferably, it is 0.5 mass%-5 mass%.
本発明に用いられる2−メタクリロイルオキシエチルホスホリルコリン(以下、MPCという。)と疎水性モノマーとの共重合体(以下、MPCコポリマーという。)は親水性と疎水性のバランスを調節したリン脂質ポリマーである。 A copolymer of 2-methacryloyloxyethyl phosphorylcholine (hereinafter referred to as MPC) and a hydrophobic monomer (hereinafter referred to as MPC copolymer) used in the present invention is a phospholipid polymer in which the balance between hydrophilicity and hydrophobicity is adjusted. is there.
前記MPCコポリマーは、下記式(1)で示される。
The MPC copolymer is represented by the following formula (1).
MPCコポリマーは、MPCと疎水性モノマーとを、常法に従い重合したものである。 The MPC copolymer is obtained by polymerizing MPC and a hydrophobic monomer according to a conventional method.
また、前記疎水性モノマーとしては、MPCと共重合体を形成し得るものであれば特に制限されない。例えば、メチルメタクリレート、エチルメタクリレート、n−ブチルメタクリレート、2−エチルヘキシルメタクリレート等のメタクリル酸エステル、メチルアクリレート、エチルアクリレート、n−ブチルアクリレート、2−エチルヘキシルアクリレート等のアクリル酸エステル、スチレン、アクリロニトリル等が挙げられる。 The hydrophobic monomer is not particularly limited as long as it can form a copolymer with MPC. For example, methacrylic acid esters such as methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, 2-ethylhexyl methacrylate, acrylic acid esters such as methyl acrylate, ethyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate, styrene, acrylonitrile, etc. It is done.
MPCコポリマーの配合量は、化粧料全量中0.01〜5質量%、好ましくは0.1〜2.5%である。0.01質量%未満では、効果が十分でなく、5質量%を超えて配合しても効果の増加は望めない。 The compounding quantity of MPC copolymer is 0.01-5 mass% in the cosmetics whole quantity, Preferably it is 0.1-2.5%. If it is less than 0.01% by mass, the effect is not sufficient, and even if it exceeds 5% by mass, an increase in the effect cannot be expected.
本発明に用いられるMPCコポリマーは、市販品を用いることが可能であり、市販品の例としては、例えば、日本油脂株式会社製、商標名「LIPIDURE−PMB」等が挙げられる。 Commercially available products can be used for the MPC copolymer used in the present invention, and examples of commercially available products include trade name “LIPIDURE-PMB” manufactured by NOF Corporation.
本発明に用いられる大豆を発酵処理することで得られた高粘性たんぱく質水溶液は、ダイズGlycine max Merrill(Leguminosae)の種子をナットウ菌Bacillus natto Sawamuraで発酵して作った納豆の20%エタノール溶液エキスに無水エタノールを加えて析出する塊状粘質物を10%エタノール溶液に分散させて得られる液である。 The highly viscous protein aqueous solution obtained by fermenting soybean used in the present invention is a 20% ethanol solution extract of natto made by fermenting soybean Glycine max Merrill (Leguminosae) seeds with Bacillus Natto Sawamura. It is a liquid obtained by adding bulk ethanol that is precipitated by adding absolute ethanol to a 10% ethanol solution.
大豆を発酵処理することで得られた高粘性たんぱく質水溶液の配合量は、化粧料全量中0.01〜10質量%、好ましくは、0.1〜5%である。0.01質量%未満では効果が十分でなく、10質量%を超えて配合しても効果の増加は望めない。 The compounding quantity of the highly viscous protein aqueous solution obtained by fermenting soybean is 0.01-10 mass% in cosmetics whole quantity, Preferably, it is 0.1-5%. If it is less than 0.01% by mass, the effect is not sufficient, and even if it exceeds 10% by mass, an increase in the effect cannot be expected.
本発明に用いられる大豆を発酵処理することで得られた高粘性たんぱく質水溶液は、市販品を用いることが可能であり、例えば、一丸ファルコス株式会社製、商標名「フィトコラージュ」等が挙げられる。 Commercially available products can be used for the high-viscosity protein aqueous solution obtained by fermenting soybeans used in the present invention, for example, trade name “Phytocollage” manufactured by Ichimaru Falcos Co., Ltd. and the like.
本発明に用いられるツボクサエキスは、例えば、ツボクサの葉及び茎からエタノール又はプロピレングリコール溶液にて抽出して得られるエキスである。 The boxweed extract used in the present invention is, for example, an extract obtained by extraction from leaves and stems of boxweed with an ethanol or propylene glycol solution.
ツボクサエキスの配合量は、化粧料全量中0.01〜10質量%、好ましくは、0.1〜5%である。0.01質量%未満では効果が十分でなく、10質量%を超えて配合しても効果の増加は望めない。 The compounding amount of the communis extract is 0.01 to 10% by mass, preferably 0.1 to 5% in the total amount of the cosmetic. If it is less than 0.01% by mass, the effect is not sufficient, and even if it exceeds 10% by mass, an increase in the effect cannot be expected.
本発明の効果を損なわない範囲で、界面活性剤、保湿剤、酸化防止剤、防腐剤、香料、着色剤、キレート剤、増粘剤等を配合することができる。 As long as the effects of the present invention are not impaired, a surfactant, a humectant, an antioxidant, an antiseptic, a fragrance, a colorant, a chelating agent, a thickener and the like can be blended.
以下、実施例を挙げて本発明を具体的に説明する。なお、本発明はこれらの実施例に限定されるものではない。 Hereinafter, the present invention will be specifically described with reference to examples. The present invention is not limited to these examples.
本発明品1,2、3と比較例1,2の化粧水を調製し、そのべたつき感、しっとり感を下記評価基準に基づき評価した。 The lotions of the present invention products 1, 2 and 3 and Comparative Examples 1 and 2 were prepared, and their stickiness and moist feeling were evaluated based on the following evaluation criteria.
[処方](%)
[製造方法]
A.リン酸−L−アスコルビルマグネシウムと精製水の50部を混合溶解する。
B.1,3−ブチレングリコールと濃グリセリン及びパラオキシ安息香酸メチルを混合溶解する。
C.AとB及び残りの成分を混合溶解する。[Prescription] (%)
[Production method]
A. Mix and dissolve 50 parts of phosphoric acid-L-ascorbyl magnesium and purified water.
B. Mix and dissolve 1,3-butylene glycol, concentrated glycerin and methyl paraoxybenzoate.
C. A and B and the remaining components are mixed and dissolved.
[評価方法]
40代〜60代の女子、計100名のパネルに各試験品を塗布してもらい、塗布時におけるべたつき、しっとりを次の評価基準で判定してもらった。[Evaluation methods]
Each test product was applied to a panel of 100 girls in their 40s to 60s, and the stickiness and moistness at the time of application were judged according to the following evaluation criteria.
[評価基準]
[Evaluation criteria]
[評価結果]
[Evaluation results]
上記の評価結果に示されるように、ビタミンC又はビタミンC誘導体を主成分とし、他の成分2−メタクリロイルオキシエチルホスホリルコリンと疎水性モノマーとの共重合体及び大豆を発酵処理することで得られた高粘性たんぱく質水溶液、更には、ツボクサエキスを含有することにより、べたつきを抑えたビタミンC又はビタミンC誘導体を主成分とする化粧料を完成した。 As shown in the above evaluation results, vitamin C or a vitamin C derivative as a main component, obtained by fermenting a copolymer of other component 2-methacryloyloxyethyl phosphorylcholine and a hydrophobic monomer and soybean By containing a high-viscosity protein aqueous solution and further a camellia extract, a cosmetic comprising vitamin C or a vitamin C derivative as a main component with reduced stickiness was completed.
化粧水:次に示す処方及び下記製法で化粧水を調製した。
[処方](%)
(1)グリセリン5.0(2)1,3−ブチレングリコール10(3)エチルアルコール1.0(4)リン酸−L−アスコルビルマグネシウム3.0(5)大豆を発酵処理することで得られた高粘性たんぱく質水溶液5(6)2−メタクリロイルオキシエチルホスホリルコリン・メタクリル酸ブチル共重合体掖0.1(7)防腐剤適量(8)精製水残量
[製造方法]
A.グリセリン、1,3−ブチレングリコール、エチルアルコール及び防腐剤を混合溶解する。
B.リン酸−L−アスコルビルマグネシウムと精製水の50部を混合溶解する。
C.AとB及び残りの成分を混合して均一にし、化粧水を得た。Lotion: Lotion was prepared according to the following formulation and the following production method.
[Prescription] (%)
(1) Glycerin 5.0 (2) 1,3-butylene glycol 10 (3) Ethyl alcohol 1.0 (4) Phosphate-L-ascorbyl magnesium 3.0 (5) Obtained by fermenting soybeans High viscosity protein aqueous solution 5 (6) 2-methacryloyloxyethyl phosphorylcholine / butyl methacrylate copolymer 掖 0.1 (7) preservative appropriate amount (8) remaining amount of purified water [production method]
A. Glycerin, 1,3-butylene glycol, ethyl alcohol and preservative are mixed and dissolved.
B. Mix and dissolve 50 parts of phosphoric acid-L-ascorbyl magnesium and purified water.
C. A, B and the remaining ingredients were mixed and made uniform to obtain a skin lotion.
化粧水:次に示す処方及び下記製法で化粧水を調製した。
[処方](%)
(1)グリセリン5.0(2)1,3−ブチレングリコール10(3)エチルアルコール1.0(4)L−アスコルビン酸2−グルコシド2.0(5)大豆を発酵処理することで得られた高粘性たんぱく質水溶液1(6)2−メタクリロイルオキシエチルホスホリルコリン・メタクリル酸ブチル共重合体液1.5(7)ツボクサエキス0.1(8)防腐剤適量(9)精製水残量
[製造方法]
A.グリセリン、1,3−ブチレングリコール、エチルアルコール及び防腐剤を混合溶解する。
B.L−アスコルビン酸2−グルコシドと精製水の50部を混合溶解する。
C.AとB及び残りの成分を混合して均一にし、化粧水を得た。Lotion: Lotion was prepared according to the following formulation and the following production method.
[Prescription] (%)
(1) glycerin 5.0 (2) 1,3-butylene glycol 10 (3) ethyl alcohol 1.0 (4) L-ascorbic acid 2-glucoside 2.0 (5) obtained by fermenting soybeans High viscosity protein aqueous solution 1 (6) 2-methacryloyloxyethyl phosphorylcholine / butyl methacrylate copolymer liquid 1.5 (7) Clover extract 0.1 (8) preservative appropriate amount (9) remaining amount of purified water [production method]
A. Glycerin, 1,3-butylene glycol, ethyl alcohol and preservative are mixed and dissolved.
B. L-ascorbic acid 2-glucoside and 50 parts of purified water are mixed and dissolved.
C. A, B and the remaining ingredients were mixed and made uniform to obtain a skin lotion.
クリーム
[処方](%)
(1)ステアリン酸3(2)セタノール3(3)ミツロウ3(4)ワセリン3(5)スクワラン10(6)モノステアリン酸POE(20)ソルビタン2(7)モノステアリン酸ソルビタン1(8)マガデミアナッツ油6(9)1,3−ブチレングリコール7(10)リン酸−L−アスコルビルマグネシウム3.0(11)大豆を発酵処理することで得られた高粘性たんぱく質水溶液0.1(12)2−メタクリロイルオキシエチルホスホリルコリン・メタクリル酸ブチル共重合体液0.1(13)ツボクサエキス1(14)防腐剤適量(15)精製水残量
[製造方法]
A.ステアリン酸、セタノール、ミツロウ、ワセリン、スクワラン、モノステアリン酸POE(20)ソルビタン、モノステアリン酸ソルビタン、マガデミアナッツ油を加熱混合し、80℃に保つ。
B.残りの成分を溶解混合後、80℃に保つ。
C.BにAをすばやく加えて混合し、均一に乳化する。Cream [Prescription] (%)
(1) stearic acid 3 (2) cetanol 3 (3) beeswax 3 (4) petrolatum 3 (5) squalane 10 (6) monostearic acid POE (20) sorbitan 2 (7) sorbitan monostearate 1 (8) Maga Demia nut oil 6 (9) 1,3-butylene glycol 7 (10) phosphate-L-ascorbyl magnesium 3.0 (11) Highly viscous protein aqueous solution 0.1 (12) obtained by fermenting soybeans 2-Methacryloyloxyethyl phosphorylcholine / butyl methacrylate copolymer solution 0.1 (13) Clover extract 1 (14) Preservative appropriate amount (15) Remaining amount of purified water [Production method]
A. Stearic acid, cetanol, beeswax, petrolatum, squalane, monostearic acid POE (20) sorbitan, sorbitan monostearate, and Magaemia nut oil are mixed by heating and maintained at 80 ° C.
B. After the remaining components are dissolved and mixed, they are kept at 80 ° C.
C. A is quickly added to B, mixed and uniformly emulsified.
Claims (3)
Priority Applications (1)
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JP2003436491A JP2005179326A (en) | 2003-12-15 | 2003-12-15 | Cosmetic |
Applications Claiming Priority (1)
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JP2003436491A JP2005179326A (en) | 2003-12-15 | 2003-12-15 | Cosmetic |
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JP2005179326A true JP2005179326A (en) | 2005-07-07 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120328597A1 (en) * | 2009-03-11 | 2012-12-27 | Jing Cheng | Topical Compositions Comprising Fermented Extracts of Traditional Chinese Medicinal (TCM) Ingredients, and Methods of Making and Using Same |
Citations (13)
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JPS58225003A (en) * | 1982-06-23 | 1983-12-27 | Ichimaru Fuarukosu Kk | Cosmetic containing extracted material for natto (fermented soybean) |
JPS58224645A (en) * | 1982-06-23 | 1983-12-27 | Ichimaru Fuarukosu Kk | Preparation of extracted material of natto (fermented soybean) |
JPH08133952A (en) * | 1994-11-07 | 1996-05-28 | Shiseido Co Ltd | Skin preparation for external use |
JPH0952848A (en) * | 1995-08-07 | 1997-02-25 | Pola Chem Ind Inc | Skin preparation for external use |
JP2000034219A (en) * | 1998-07-17 | 2000-02-02 | Shiseido Co Ltd | Preparing for external use for skin |
JP2000034218A (en) * | 1998-07-17 | 2000-02-02 | Shiseido Co Ltd | Preparing for external use for skin |
JP2000034217A (en) * | 1998-07-17 | 2000-02-02 | Shiseido Co Ltd | Preparation for external use for skin |
JP2001064152A (en) * | 1999-06-23 | 2001-03-13 | Nof Corp | Skin cosmetic |
JP2001064151A (en) * | 1999-06-23 | 2001-03-13 | Nof Corp | Skin cosmetic |
JP2002104919A (en) * | 2000-09-29 | 2002-04-10 | Shiseido Co Ltd | Skin care preparation |
JP2002255730A (en) * | 2001-03-01 | 2002-09-11 | Chifure Keshohin:Kk | Cosmetic |
JP2003073251A (en) * | 2001-08-31 | 2003-03-12 | Shiseido Co Ltd | Skin care preparation |
JP2003081741A (en) * | 2001-09-13 | 2003-03-19 | Nikko Seiyaku Kk | Skin care preparation |
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2003
- 2003-12-15 JP JP2003436491A patent/JP2005179326A/en active Pending
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58225003A (en) * | 1982-06-23 | 1983-12-27 | Ichimaru Fuarukosu Kk | Cosmetic containing extracted material for natto (fermented soybean) |
JPS58224645A (en) * | 1982-06-23 | 1983-12-27 | Ichimaru Fuarukosu Kk | Preparation of extracted material of natto (fermented soybean) |
JPH08133952A (en) * | 1994-11-07 | 1996-05-28 | Shiseido Co Ltd | Skin preparation for external use |
JPH0952848A (en) * | 1995-08-07 | 1997-02-25 | Pola Chem Ind Inc | Skin preparation for external use |
JP2000034219A (en) * | 1998-07-17 | 2000-02-02 | Shiseido Co Ltd | Preparing for external use for skin |
JP2000034218A (en) * | 1998-07-17 | 2000-02-02 | Shiseido Co Ltd | Preparing for external use for skin |
JP2000034217A (en) * | 1998-07-17 | 2000-02-02 | Shiseido Co Ltd | Preparation for external use for skin |
JP2001064152A (en) * | 1999-06-23 | 2001-03-13 | Nof Corp | Skin cosmetic |
JP2001064151A (en) * | 1999-06-23 | 2001-03-13 | Nof Corp | Skin cosmetic |
JP2002104919A (en) * | 2000-09-29 | 2002-04-10 | Shiseido Co Ltd | Skin care preparation |
JP2002255730A (en) * | 2001-03-01 | 2002-09-11 | Chifure Keshohin:Kk | Cosmetic |
JP2003073251A (en) * | 2001-08-31 | 2003-03-12 | Shiseido Co Ltd | Skin care preparation |
JP2003081741A (en) * | 2001-09-13 | 2003-03-19 | Nikko Seiyaku Kk | Skin care preparation |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120328597A1 (en) * | 2009-03-11 | 2012-12-27 | Jing Cheng | Topical Compositions Comprising Fermented Extracts of Traditional Chinese Medicinal (TCM) Ingredients, and Methods of Making and Using Same |
US8580319B2 (en) * | 2009-03-11 | 2013-11-12 | Elc Management, Llc | Topical compositions comprising fermented extracts of traditional chinese medicinal (TCM) ingredients, and methods of making and using same |
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