JPS6078913A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPS6078913A
JPS6078913A JP18727883A JP18727883A JPS6078913A JP S6078913 A JPS6078913 A JP S6078913A JP 18727883 A JP18727883 A JP 18727883A JP 18727883 A JP18727883 A JP 18727883A JP S6078913 A JPS6078913 A JP S6078913A
Authority
JP
Japan
Prior art keywords
ascorbic acid
sulfate
aging
vitamin
tocopherol
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
Application number
JP18727883A
Other languages
Japanese (ja)
Inventor
Akira Akiyasu
秋保 暁
Yumiko Suzuki
裕美子 鈴木
Minoru Fukuda
実 福田
Keisuke Nakajima
啓介 中嶋
Atsuko Igarashi
五十嵐 敦子
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.)
Shiseido Co Ltd
Original Assignee
Shiseido Co Ltd
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 Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP18727883A priority Critical patent/JPS6078913A/en
Publication of JPS6078913A publication Critical patent/JPS6078913A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/67Vitamins
    • A61K8/676Ascorbic acid, i.e. vitamin C
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/02Preparations for care of the skin for chemically bleaching or whitening the skin

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:To provide a cosmetic obtained by compounding L-ascorbic acid-2- sulfate or its salt with vitamin E, and having improved transcutaneous permeability, synergistically increased beautifying effect, and improved effect to prevent the aging, without lowering the stability of the former component. CONSTITUTION:A cosmetic having remarkably improved beautifying and aging- preventive effect can be produced by compounding L-ascorbic acid-2-sulfate or its salt (e.g. salt of Na, K, Mg, Ca, etc.) and a vitamin E compound (e.g. alpha-, beta-, gamma-tocopherol, tocopherol acetate, etc.). The use of 10wt% L-ascorbic acid-2- sulfate and 2wt% vitamin E is sufficient to attain the above effects. The combined use of the above components enables the increase in the transcutaneous permeability and the remarkable improvement in the spots and freckles without lowering the stability of L-ascorbic acid-2-sulfate. The content of soluble collagen in the living tissue can be increased to prevent the aging of the body.

Description

【発明の詳細な説明】 本発明は、美白効果、老化防止効果が著しく改良された
新規な化粧料に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel cosmetic material with significantly improved whitening and anti-aging effects.

従来−美白化粧料は、じみやそばかすの原因となる日焼
けした皮ハ号などを美白するために主として使用されて
おり、化粧料の中でも消費者の期待が大変強いものであ
る〇 アスコルビン酸はチロシンからメラニンヲ’4= 成す
るチロシナーゼの作用を阻害し、又、生成している濃色
酸化型メラニンを淡色還元型メラニンに戻す作用を有し
、皮IF7の美白化、しみ、そばかす、黒皮症、肝斑等
の治療、改碧に有効な化合物であることは周知であるが
、熱や光に対して極めて不安定で酸化され易い性質を有
し、特に水分を含有する化粧料中においては分解し易く
、着色を招き易い。そのためアスコルビン酸を安定化す
る目的でアスコルビン酸を高級1ffi 1IJj酸や
りん酸のエステル体として配合したり、抗酸化剤もしく
は還元剤を使用添加することが提案されているが、アス
コルビン酸を安定化すればする程、美白効果が薄れ、配
合量を増せば皮lIす刺激が出現するといった問題点が
あった。
Traditionally - Whitening cosmetics are mainly used to whiten sunburned skin that causes age spots and freckles, and consumers have very high expectations among cosmetics. Ascorbic acid is tyrosine. It inhibits the action of tyrosinase that produces melanin, and also has the effect of returning the dark oxidized melanin to the light reduced melanin, resulting in skin whitening, age spots, freckles, and melasma. Although it is well known that it is an effective compound for the treatment of melasma and other skin conditions, it is extremely unstable and easily oxidized by heat and light, and is particularly useful in cosmetics containing water. Easy to decompose and cause discoloration. Therefore, in order to stabilize ascorbic acid, it has been proposed to blend ascorbic acid as an ester of higher 1ffi 1IJj acid or phosphoric acid, or to add an antioxidant or reducing agent. The more you use it, the more the whitening effect will fade, and if you increase the amount, it will cause irritation to your skin.

又、最近になって、L−アスコルビン酸の2位の水酸基
を硫酸エステル化したL−アスコルビン酸−2−硫酸が
、開発され、安定化の点では大きく改良された。しかし
ながら、経皮透過性の点で未だ検討の余地が残されてい
、るのが現状である。
Recently, L-ascorbic acid-2-sulfuric acid, which is obtained by converting the hydroxyl group at the 2-position of L-ascorbic acid into a sulfuric acid ester, has been developed, and has been greatly improved in terms of stabilization. However, the current situation is that there is still room for investigation in terms of transdermal permeability.

最近ではα−トコフェロールに美白効果が認められたと
する報告もなされているが、本発明者らの追試によれば
効果は無いに等しいものであった〇老化防止効果につい
ても、ビタミンEに効果があると言われているが未だ不
十分なものであった。
Recently, there have been reports that α-tocopherol has a whitening effect, but according to the inventors' follow-up tests, the effect was negligible.As for the anti-aging effect, vitamin E has no effect. Although it is said that there is, it is still insufficient.

本発明者らは、こうした事情にがんかみ真に優れた美白
及び老化防止効果を有する化粧料を得るべく鋭意研究を
重ねた結果、L−アスコルビン酸−2−硫酸および/ま
たは、その塩芦壬タミンE類とを化粧料に配合すること
により、L−アスコルビン酸−2−硫酸の安定性を□損
うことなく、経皮透過性が増加し、しみ、そばかす、色
黒などが著しく改善され、美白効果が相乗的に増大し、
さらに老化を著しく防止し得ることを見い出し、本発明
を完成するに至った〇 すなわち、本発明は、L−アスコルビン酸−2−硫酸、
およびその塩類よりなる群から選ばれた1種又は2種以
上とを含有することを特徴とする化粧料である。
In view of these circumstances, the present inventors have conducted extensive research to obtain cosmetics with truly excellent whitening and anti-aging effects. By incorporating Mitamin E into cosmetics, transdermal permeability increases without impairing the stability of L-ascorbic acid-2-sulfuric acid, and stains, freckles, dark skin, etc. are significantly improved. The whitening effect increases synergistically.
Furthermore, it was discovered that aging can be significantly prevented, leading to the completion of the present invention.In other words, the present invention provides L-ascorbic acid-2-sulfuric acid,
and one or more selected from the group consisting of salts thereof.

(以下余白) 次に本発明の構成について述べる。(Margin below) Next, the configuration of the present invention will be described.

本発明に使用するL−アスコルビン酸−2−硫酸はL−
アスコルビン酸の2位の水酸基を硫酸エステル化したも
のである。本溌明に使用するL−アスコルビン酸−2−
硫酸の塩としてはNa、K、Mg、Oaなどの塩をあげ
ることができる。
The L-ascorbic acid-2-sulfuric acid used in the present invention is L-
It is obtained by converting the hydroxyl group at the 2-position of ascorbic acid into a sulfuric acid ester. L-ascorbic acid-2- used in Honjomei
Examples of sulfuric acid salts include Na, K, Mg, and Oa salts.

L−アスコルビン酸−2−硫酸又はその塩は、化粧量中
に、0001重量%以上配合すると効果があられれ、本
発明の効果を発揮するためには迫重量%程度で十分であ
る。
L-ascorbic acid-2-sulfuric acid or its salt is effective when incorporated in the amount of cosmetics in an amount of 0,001% by weight or more, and approximately 1% by weight is sufficient to exhibit the effects of the present invention.

本発明に使用するビタミンE類としては、例えハ、α−
トコフェロール、β−トフフェロール、γ−トコフェロ
ール、δ−トコフェロール、酢酸トコフェロール、又ハ
ニコチン酸トコフェロール等が挙げられ、化粧料中に0
001重量%以上配合すると相乗的な効果を発揮し、2
重量%程度で十分である。
Examples of vitamin E used in the present invention include C, α-
Examples include tocopherol, β-tocopherol, γ-tocopherol, δ-tocopherol, tocopherol acetate, and tocopherol honeynicotinate, which contain 0% in cosmetics.
001% by weight or more exhibits a synergistic effect,
About % by weight is sufficient.

本発明の化粧料は、上記の必須成分の他に通常化粧料に
配合される成分たとえば紫外線吸収剤、湿潤剤、防腐剤
、界面活性剤、香料、色素等を、本発明の効果を損わな
い範囲で適宜組′合わせ、使用することができる。
In addition to the above-mentioned essential ingredients, the cosmetics of the present invention contain ingredients that are usually added to cosmetics, such as ultraviolet absorbers, humectants, preservatives, surfactants, fragrances, pigments, etc., without impairing the effects of the present invention. They can be used in appropriate combinations within the range.

次に実施例をあげて本発明をさらに詳細に説明する。本
発明はこれにより限定されるものではない。配合量は重
量(%)である。
Next, the present invention will be explained in more detail with reference to Examples. The present invention is not limited thereby. The blending amount is by weight (%).

実施例に先だち試験法、判定法を説明する。Prior to examples, test methods and judgment methods will be explained.

く皮、膚透過試験) (試験法) 実験動物として、ハートレイ系雄のモルモット(300
〜3509 )を使用した。実験41」前に脱毛処理し
た背部皮1葭5 Cm2に、試料ローション50〜を塗
布後、直ちにプラスチックフィルムで閉塞した。
(Test method) Hartley male guinea pigs (300
~3509) was used. After applying 50~ of the sample lotion to 5 cm2 of dorsal skin that had been depilated before Experiment 41, it was immediately closed with a plastic film.

a $i 24 時間[1にJg殺し、エタノール、次
いで水で湿した脱脂綿で皮11%1表面をふきとった後
・角層をセロテープで傾回剥離した。次いで支店を切り
取り、直ちに凍結し、皮下組織を除去後ミクロトームに
て真皮側より皮119面に平行に25岸の薄切片を作成
し、皮1台深度bμm〜100μmまでを表皮細胞層と
し、100μtn %−1500μmまどを真皮層とし
て、それぞれの切片中のL−アスコルビンff1−2−
 硫酸の量を測定し、それをもって経皮透過量とした。
a $i 24 hours [1 Jg] After wiping the surface of the skin with absorbent cotton moistened with ethanol and water, the stratum corneum was peeled off by tilting with cellophane tape. Next, the branch was cut out, immediately frozen, and after removing the subcutaneous tissue, 25 thin sections were made from the dermis side parallel to the 119th surface of the skin using a microtome. %-1500μm window as dermal layer, L-ascorbine ff1-2- in each section
The amount of sulfuric acid was measured and used as the transdermal permeation amount.

なお、経皮透過量は、モルモット3匹の平均値をとった
The transdermal permeation amount was the average value of three guinea pigs.

(判 定) ◎:試料塗布滉時間後に表皮細胞層及び真皮層に経皮透
過したL−アスコルビン酸−2−硫酸の量が塗布量の1
0%以上の場合。
(Judgment) ◎: The amount of L-ascorbic acid-2-sulfuric acid that permeated through the skin into the epidermal cell layer and dermal layer after the sample application period was 1 of the applied amount.
If it is 0% or more.

○: 〃 塗布量の5〜lO%の場合。○: 5 to 10% of the coating amount.

×:〃 塗布量の5%以下の場合。×: 5% or less of the coating amount.

(以下衆目) 〈累積塗布による美白効果試験〉 (試験方法) 色黒、しみ、そばかす等に悩む被試験n、lBY釦名と
して1つの試料ローションを朝夕、3ケ月間毎日顔面に
塗布し、3力月目にその美白効果を調べた。
(Hereinafter referred to as general) <Test on whitening effect by cumulative application> (Test method) One sample lotion was applied to the face morning and evening every day for 3 months as a test subject suffering from dark skin, age spots, freckles, etc. for 3 months. We investigated its whitening effect on a monthly basis.

(判定基準) 著効:色素沈着がほとんど目立たなくなった。(Judgment criteria) Significant results: Pigmentation is almost invisible.

有効:非常にうずくなった。Valid: Very tingling.

やや有効:ややうずくなった。Slightly effective: Slightly tingling.

無効:変化なし。Invalid: No change.

(判 定〕 ◎:被験者のうち著効、有効の示す割合(イ」効率)が
80%以上。
(Judgment) ◎: The percentage of subjects showing significant or effective response (A) efficiency is 80% or more.

Q : 50%〜80%。Q: 50% to 80%.

×:50%以下。×: 50% or less.

くコラーゲン合成試験〉 コラーゲンとはホ乳類の真皮組織などを構成する繊維状
タンパク質を表わし、可溶性コラーゲンと不溶性コラー
ゲンとがある。一般に、老化の原因として不溶性コラー
ゲンの増加があげられてしる。すなわち、可溶性コラー
ゲンを増やし、不溶性コラーゲンを減らすことにより老
化を防ぎ、木々しい肌を保つことができると考えら截る
Collagen Synthesis Test Collagen is a fibrous protein that constitutes the dermal tissue of mammals, and there are two types: soluble collagen and insoluble collagen. Generally, an increase in insoluble collagen is cited as a cause of aging. In other words, by increasing soluble collagen and decreasing insoluble collagen, it is believed that aging can be prevented and skin can be maintained with a fresh appearance.

(試験方法) 実験動物としてウィスター系雄ラットを使用した。脱毛
処理した背部皮膚5X 5 cJに試料を05m1ずつ
1日1回7日間塗布した。8日日に動物を層殺後皮1e
をとり出し1皮下組織を除去後、表皮・真皮層のみをホ
モジネートした。ホモジネートより可溶性コラーゲン及
び不溶性コラーゲンを抽出し、ハイドロオキシプロリン
量として定量をイアなった。
(Test method) Wistar male rats were used as experimental animals. 05 ml of the sample was applied once a day for 7 days to 5×5 cJ of the back skin that had been subjected to depilation treatment. On the 8th day, the animal was sacrificed and the skin 1e
After removing the subcutaneous tissue, only the epidermis and dermis layers were homogenized. Soluble collagen and insoluble collagen were extracted from the homogenate and quantified as the amount of hydroxyproline.

(判 定) ◎:未塗布の場合のDJ溶性コラーゲンに対する塗布し
た場合の可溶性コラーゲンの増加比と、未塗布の場合の
不溶性コラーゲンに対する塗布した場合の不溶性コラー
ゲンの減少比との和が50%以上。
(Judgment) ◎: The sum of the increase ratio of soluble collagen when applied to DJ soluble collagen when not applied and the decrease ratio of insoluble collagen when applied to DJ soluble collagen when not applied is 50% or more. .

△: 〃 田〜50%。△: ~50%.

X: //21:4%以下。X: //21: 4% or less.

−〇一 実施例1〜3、比較例1〜2について述べる表1の配合
組成よりなるローションを調整し、その経皮透過性およ
び累積塗布による美白効果について調べた。
-〇1 A lotion having the composition shown in Table 1 described in Examples 1 to 3 and Comparative Examples 1 to 2 was prepared, and its transdermal permeability and whitening effect upon cumulative application were investigated.

製法は、以下の方法で調整した。即ち95%エチルアル
コール109に、酢酸トフフェロール必要鼠、!:、F
OR(財)ラウリルエーテル0.59および香料を混合
し、次いで、この中に、グリセリン2すとプロピレング
リコール1qと、クエンm O,29、L−アスコルビ
ン酸−2=硫酸を加え、史に蒸留水を、全重量が100
 gになるように加え混合してシ1f整した。
The manufacturing method was adjusted as follows. That is, 95% ethyl alcohol 109 and topherol acetate are required! :,F
Mix 0.59% of OR (Incorporated) lauryl ether and fragrance, then add 2 s of glycerin, 1 q of propylene glycol, 29 citric acid, 29 L-ascorbic acid, and sulfuric acid. water, total weight 100
g, mixed, and prepared in 1f.

(以 下余白) 表1 表1から明らかな様に、本発明の化粧料は美白効果、老
化防止効果に優れる新規な化粧料である。
(Margin below) Table 1 As is clear from Table 1, the cosmetic of the present invention is a novel cosmetic with excellent whitening and anti-aging effects.

(以下余白) 実施例4 乳 液 つぎの処方に従い、常法により乳液を製造した。(Margin below) Example 4 Milk liquid A milky lotion was produced by a conventional method according to the following recipe.

ステアリン酸 2.0 セタノール LO ワセリン 3゜ ラノリンアルコール 2+。Stearic acid 2.0 Setanol LO Vaseline 3゜ Lanolin alcohol 2+.

流動パラフィン a。Liquid paraffin a.

スクワラン 3.0 エス力ロール507 2+0 α−トコフェロール 0.06 L−アスコルビン酸−2−硫1!i!2Na O,00
1P OIn(10)モ/オレート z5トリエタノー
ルアミン 1.0 プロピレングリコニル 5゜ 香 料 適量 防腐剤 適量 蒸留水 70.439 (以下余白) 実施例5 栄養クリーム つぎの処方に従い、常法によりクリームを製造した。
Squalane 3.0 S-Riki Roll 507 2+0 α-tocopherol 0.06 L-ascorbic acid-2-sulfur 1! i! 2Na O,00
1P OIn(10) mo/oleate z5 Triethanolamine 1.0 Propylene glyconyl 5°Fragrance Appropriate amount Preservative Appropriate amount Distilled water 70.439 (Left below) Example 5 Nutritional cream Cream was made in a conventional manner according to the following recipe. Manufactured.

ステアリン酸 zO ステアリルアルコール 7.0 還元ラノリン zO スクワラン 5.0 オクチルドデカノール 60 ポリオキシエチレンセチルエーテル(25EQ) 3.
0親油型モノステアリン酸グリセリン 2.0ニコチン
酸トコフエロール 0.01 L−アスコルビン酸−2−硫酸 005プロピレングリ
コール 50 香 料 適量 防腐剤 適量 蒸留水 67.94 (以下余白ン 実施例6 パ ッ り つぎの処方に従い、常法によりパックを製造した。
Stearic acid zO Stearyl alcohol 7.0 Reduced lanolin zO Squalane 5.0 Octyldodecanol 60 Polyoxyethylene cetyl ether (25EQ) 3.
0 Lipophilic glyceryl monostearate 2.0 Tocopherol nicotinate 0.01 L-ascorbic acid-2-sulfuric acid 005 Propylene glycol 50 Flavor Appropriate amount Preservative Appropriate amount Distilled water 67.94 (Example 6 in the margin below) A pack was manufactured by a conventional method according to the following recipe.

カオリン 691 タ ル り 190 プロピレングリコール 50 酢酸カルシウム α01 尿 酸 0.5 L−アスコルビン酸−2−硫酸 5.0α−トコフェロ
ール 1.0 香 料 0.39 (以 1・ 余目〕 実施例7 バ ス タ つぎの処方に従い、常法によりパスタを製造したO ポリオキシエチレンソルビクンジステアレー) 15.
0ポリオキシエチレンソルビタンモノオレート2−Oビ ア 洲≠ セ ル 1.0 グリセリン 100 ヒドロキシエチル七ルロース 4.0 L−アスコルビン酸−2−硫酸 10 L−アスコルビン酸−2−硫酸Mり 30α−トコフェ
ロール 05 酢酸トコフエロール 05 香 料 適量 防腐剤 適量 精製水 630 実施例4〜7により得られる化粧料は英白効果1老化防
止効果に優れていた。
Kaolin 691 Tart 190 Propylene glycol 50 Calcium acetate α01 Uric acid 0.5 L-ascorbic acid-2-sulfuric acid 5.0 α-tocopherol 1.0 Fragrance 0.39 (1. Extra) Example 7 Batha 15. Pasta was produced according to the following recipe by a conventional method.
0 Polyoxyethylene sorbitan monooleate 2-O Via ≠ Cell 1.0 Glycerin 100 Hydroxyethyl heptalulose 4.0 L-Ascorbic acid-2-sulfuric acid 10 L-Ascorbic acid-2-sulfuric acid M 30 α-Tocopherol 05 Tocopherol acetate 05 Fragrance Appropriate amount Preservative Appropriate amount Purified water 630 The cosmetics obtained in Examples 4 to 7 were excellent in Eihaku effect 1 anti-aging effect.

特許出願人 株式会社 資 生 堂Patent applicant Shiseido Co., Ltd.

Claims (2)

【特許請求の範囲】[Claims] (1)L−アスコルビン酸−2−硫酸、およびその塩類
よりなる群から選ばれた1種又は2種以上と、ビタミン
E類の1種または2種以上とを含有することを特徴とす
る化粧料。
(1) Cosmetics characterized by containing one or more types selected from the group consisting of L-ascorbic acid-2-sulfuric acid and its salts and one or more types of vitamin E. fee.
(2)L−アスコルビン酸−2−硫酸の塩類がHa。 Kなどのアルカリ金属及びMg、Caなどのアルカリ 土類金属の塩である特許請求範囲第1項記載の化粧料。 フェロール、又はニコチン酸トコフェロールであ(− る特許請求範囲第1項ないし第2項のいずれかに記載の
化粧料。
(2) Salts of L-ascorbic acid-2-sulfuric acid are Ha. The cosmetic according to claim 1, which is a salt of an alkali metal such as K and an alkaline earth metal such as Mg and Ca. The cosmetic according to any one of claims 1 to 2, which is ferol or tocopherol nicotinate.
JP18727883A 1983-10-06 1983-10-06 Cosmetic Pending JPS6078913A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18727883A JPS6078913A (en) 1983-10-06 1983-10-06 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18727883A JPS6078913A (en) 1983-10-06 1983-10-06 Cosmetic

Publications (1)

Publication Number Publication Date
JPS6078913A true JPS6078913A (en) 1985-05-04

Family

ID=16203196

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18727883A Pending JPS6078913A (en) 1983-10-06 1983-10-06 Cosmetic

Country Status (1)

Country Link
JP (1) JPS6078913A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01283208A (en) * 1988-05-02 1989-11-14 Nonogawa Shoji:Kk Beautifying cosmetic
WO1992007544A1 (en) * 1990-10-26 1992-05-14 Shiseido Co., Ltd. External preparation for skin
JP2000095641A (en) * 1998-09-25 2000-04-04 Kanebo Ltd Bleaching preparation

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50117945A (en) * 1974-03-02 1975-09-16

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50117945A (en) * 1974-03-02 1975-09-16

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01283208A (en) * 1988-05-02 1989-11-14 Nonogawa Shoji:Kk Beautifying cosmetic
WO1992007544A1 (en) * 1990-10-26 1992-05-14 Shiseido Co., Ltd. External preparation for skin
JP2000095641A (en) * 1998-09-25 2000-04-04 Kanebo Ltd Bleaching preparation

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