JP2902842B2 - Skin cosmetics - Google Patents
Skin cosmeticsInfo
- Publication number
- JP2902842B2 JP2902842B2 JP35249691A JP35249691A JP2902842B2 JP 2902842 B2 JP2902842 B2 JP 2902842B2 JP 35249691 A JP35249691 A JP 35249691A JP 35249691 A JP35249691 A JP 35249691A JP 2902842 B2 JP2902842 B2 JP 2902842B2
- Authority
- JP
- Japan
- Prior art keywords
- skin
- action
- astringent
- cosmetic
- parts
- 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.)
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Description
【0001】[0001]
【産業上の利用分野】本発明は、経日安定性が良好で、
優れた収斂作用及び整肌・保護作用を有する皮膚化粧料
に関する。BACKGROUND OF THE INVENTION The present invention has good day-to-day stability,
The present invention relates to a skin cosmetic having an excellent astringent action and a skin conditioning / protecting action.
【0002】[0002]
【従来の技術及び発明が解決しようとする課題】従来、
皮膚化粧料に、皮膚に対する収斂作用及び整肌・保護作
用発現の有効成分として亜鉛化合物(例えば、パラフェ
ノールスルホン酸亜鉛,酸化亜鉛)及びアルミニウム化
合物(例えば、塩化アルミニウム、塩基性塩化アルミニ
ウム等)が配合されるが、これらは皮膚刺激を伴うか、
効果が不充分である等の問題があり、満足のいくものが
得られなかった。2. Description of the Related Art
In skin cosmetics, a zinc compound (for example, zinc paraphenolsulfonate, zinc oxide) and an aluminum compound (for example, aluminum chloride, basic aluminum chloride, etc.) are contained as active ingredients for exhibiting an astringent action and a skin conditioning / protecting action on the skin. But these are accompanied by skin irritation,
There were problems such as insufficient effects, and satisfactory products could not be obtained.
【0003】このような状況に鑑み、本発明者は、柿に
含有している縮合型タンニンが極めて優れた収斂作用及
び整肌・保護作用を有し、皮膚刺激がなく、皮膚化粧料
に配合するのに非常に適した有効成分であることを見出
した(特開昭61−236713号公報)。[0003] In view of such circumstances, the inventor of the present invention has concluded that condensed tannin contained in persimmon has an extremely excellent astringent action, skin conditioning and protective action, has no skin irritation, and is incorporated into skin cosmetics. It has been found that this is an active ingredient which is very suitable for carrying out the method (JP-A-61-236713).
【0004】一方、ポリオキシエチレン付加型非イオン
界面活性剤は、ポリオキシエチレン鎖長及びアルキル鎖
長を任意に設定することができるので、乳化剤、可溶化
剤、分散剤として皮膚化粧料に汎用されている。しか
し、ポリオキシエチレン付加型非イオン界面活性剤とポ
リフェノール化合物の組合せから成る皮膚化粧料を製造
するとき、両分子間の相互作用による複合体が不溶物と
して生成するために、皮膚化粧料としての製剤機能が損
なわれ、同時に、皮膚に対する収斂作用及び整肌・保護
作用も充分に満足されないという問題を持つことが判明
した。On the other hand, polyoxyethylene-added nonionic surfactants can be used in skin cosmetics as emulsifiers, solubilizers and dispersants because the polyoxyethylene chain length and alkyl chain length can be set arbitrarily. Have been. However, when producing a skin cosmetic comprising a combination of a polyoxyethylene addition type nonionic surfactant and a polyphenol compound, a complex due to an interaction between both molecules is formed as an insoluble substance, so that the skin cosmetic is used as a skin cosmetic. It has been found that the function of the preparation is impaired, and at the same time, the astringent action on the skin and the skin conditioning / protecting action are not sufficiently satisfied.
【0005】そこで、本発明者等は、この欠点を改良せ
んとして鋭意検討した結果、ポリフェノール化合物とア
ルキルグリコシドを組合せて使用するとき、両分子間で
複合体を形成することなく、優れた製剤機能を有する皮
膚化粧料が得られることを見出し、本発明を完成した。Therefore, the present inventors have conducted intensive studies to improve this drawback, and as a result, when a polyphenol compound and an alkyl glycoside are used in combination, excellent formulation function is obtained without forming a complex between both molecules. Have been found, and have completed the present invention.
【0006】即ち、本発明は、経日安定性が良好で、優
れた収斂作用及び整肌・保護作用を有する皮膚化粧料を
提供することを目的とするものである。[0006] That is, an object of the present invention is to provide a skin cosmetic composition which has good aging stability, and has an excellent astringent action and a skin conditioning / protecting action.
【0007】[0007]
【課題を解決するための手段】上記の目的を達成するた
めに、本発明の皮膚化粧料は次のような構成をとる。即
ち、ポリフェノール化合物とアルキルグリコシドとを含
有することを特徴とする皮膚化粧料である。Means for Solving the Problems To achieve the above object, the skin cosmetic of the present invention has the following constitution. That is, a skin cosmetic comprising a polyphenol compound and an alkyl glycoside.
【0008】本発明におけるポリフェノール化合物とし
て、例えば、没食子酸、没食子酸エステル(プロピルエ
ステル、イソアミルエステル、オクチルエステル、ドデ
シルエステル等)、ピロガロール、フロログリシン、カ
テキン、エピカテキン、ガロカテキン、カテキンガレー
ト、ガロカテキンガレート、エピカテキンガレート、エ
ピガロカテキンガレート、エピガロカテキン、グルコガ
リン、プロアントシアニジン及びそのポリマー、フラボ
ン類(例えば、ルチン、クエルセチン、クエルセタギ
ン、クエルセタギチン、ゴシペチン等)、エラグ酸、ペ
ンタ−O−ガロイルグルコース、タンニン酸、ガロタン
ニン(シャクヤク抽出物のタンニン)、エラジタンニン
(ゲンノショウコ、アカメガシワ、ザクロ皮、サンシュ
ユ、詞子等から抽出した各タンニン)、縮合型タンニン
(渋柿、茶、桂皮、阿仙薬、地楡茶等から抽出した各タ
ンニン)、ウラジロガシ皮、ミズナラ皮、同堅果等から
抽出した各タンニン等を挙げることができる。Examples of the polyphenol compound in the present invention include gallic acid, gallic acid esters (propyl ester, isoamyl ester, octyl ester, dodecyl ester, etc.), pyrogallol, phloroglysin, catechin, epicatechin, gallocatechin, catechin gallate, gallocatechin. Gallate, epicatechin gallate, epigallocatechin gallate, epigallocatechin, glucogalin, proanthocyanidins and polymers thereof, flavones (eg, rutin, quercetin, quercetagine, quercetagitin, gossypetin, etc.), ellagic acid, penta-O-galloylglucose , Tannic acid, gallotannins (tannins of peonies extract), ellagitannins (extracted from genoshoko, akamegawiwa, pomegranate skin, sanshuyu, lye, etc.) Each tannin) has, condensed tannins (astringent persimmon, tea, cinnamon, Uncaria gambir Roxburgh, each tannin extracted from Chinire tea, etc.), Quercus salicina bark, oak bark, may be mentioned the tannin or the like extracted from the nuts and the like.
【0009】また、本発明におけるアルキルグリコシド
とは、炭素数8〜22のアルキル基又はアルケニル基と
1〜5個の炭素数5〜6の還元糖に由来する糖部から構
成されるもので、単糖類ではグルコース、ガラクトー
ス、キシロース、フラクトース、マンノース、リキソー
ス、アピビノース等が、2糖以上ではマルトース、キシ
ロビオース、イソマンノース、ラクトース、スクロー
ス、ラフィノース、マルトトリオース等が挙げられる。
そして、これらのうち特に好ましい原料は、コスト面か
らグルコース、フラクトース、マルトース、スクロース
である。そして、糖部が2個以上から構成されたアルキ
ルグリコシドの場合、その糖鎖の結合様式は、1−2、
1−3、1−4、1−6結合、更にα,β−ピラノシ
ド、又はフラノシド結合及びこれらが任意に混合された
ものが可能である。従って、例えばデシル−β−D−グ
リコシド、テトラデシル−α−D−フルクトシド、ドデ
シル−β−D−マルトシド、オクタデシル−α−D−ス
クロシド等が挙げられる。The alkyl glycoside in the present invention comprises an alkyl group or alkenyl group having 8 to 22 carbon atoms and a sugar moiety derived from 1 to 5 reducing sugars having 5 to 6 carbon atoms. Monosaccharides include glucose, galactose, xylose, fructose, mannose, lyxose, apivinose and the like, and disaccharides and more include maltose, xylobiose, isomannose, lactose, sucrose, raffinose, maltotriose and the like.
Particularly preferred raw materials among these are glucose, fructose, maltose and sucrose from the viewpoint of cost. And in the case of an alkyl glycoside in which the sugar moiety is composed of two or more, the sugar chain binding mode is 1-2,
1-3, 1-4, 1-6 bonds, furthermore, α, β-pyranoside or furanoside bonds and any mixture thereof are possible. Accordingly, for example, decyl-β-D-glycoside, tetradecyl-α-D-fructoside, dodecyl-β-D-maltoside, octadecyl-α-D-scroside and the like can be mentioned.
【0010】本発明の皮膚化粧料としては、例えば、化
粧水、乳液、クリーム、パック、クレンジング、洗顔
料、メイクアップベース、ファンデーション、リップク
リーム、口紅等が挙げられるが、特に、これらに限定さ
れず、他の皮膚化粧料及び医薬部外品に適用することが
できる。The skin cosmetics of the present invention include, for example, lotions, emulsions, creams, packs, cleansings, facial cleansers, makeup bases, foundations, lip balms, lipsticks and the like, but are not particularly limited thereto. And can be applied to other skin cosmetics and quasi-drugs.
【0011】[0011]
【実施例】実施例によって本発明を更に詳細に説明す
る。実施例に示す部とは、重量部を意味する。The present invention will be described in more detail with reference to examples. Parts shown in the examples mean parts by weight.
【0012】尚、実施例を詳述するに先立ち、そこで使
用する試験方法について述べる。Before describing the embodiments in detail, test methods used therein will be described.
【0013】1.経日安定性試験方法 実施例及び比較例に示した皮膚化粧料を製造直後及び4
0℃の恒温槽に密閉容器中に6ケ月間放置後(加速試
験)、外観を肉眼にて評価した。1. Daily stability test method The skin cosmetics shown in Examples and Comparative Examples were prepared immediately after production and
After standing for 6 months in a closed container in a thermostat at 0 ° C. (acceleration test), the appearance was visually evaluated.
【0014】2.有用性(皮膚への収斂作用及び整肌・
保護作用)試験方法 実施例及び比較例に示した皮膚化粧料の皮膚に対する収
斂作用に関し、荒れ肌性の者から選択された専門検査員
10名が、1日1回、7日間連続して試料の皮膚化粧料
0.3gを肌に均一に塗布して、実用テストを行った
後、8日目の皮膚の状態を判断し、次の基準で評価し
た。 5:皮膚の収斂作用は大変良い。 4:皮膚の収斂性はやや良い。 3:皮膚の収斂性は普通。 2:皮膚の収斂性はやや悪い。 1:皮膚の収斂性は悪い。 さらに、荒肌改善性の視点から整肌・保護作用に関して
も上記と同様に判断し、同様の5段階基準で評価した。
尚、10人の専門検査員による評価点の平均値を各試料
の得点とした。2. Usefulness (astringent effect on skin and skin conditioning
Protective action) Test method Regarding the astringent action of the skin cosmetics shown in the examples and comparative examples on the skin, ten specialist inspectors selected from persons with rough skin once a day for seven consecutive days After applying 0.3 g of skin cosmetics uniformly to the skin and performing a practical test, the condition of the skin on the 8th day was judged and evaluated according to the following criteria. 5: The astringent action of the skin is very good. 4: The astringency of the skin is somewhat good. 3: The astringency of the skin is normal. 2: The astringency of the skin is somewhat poor. 1: The astringency of the skin is poor. Further, from the viewpoint of improving rough skin, skin conditioning / protecting action was also determined in the same manner as described above, and evaluated based on the same five-point standard.
In addition, the average value of the evaluation points by ten specialist inspectors was used as the score of each sample.
【0015】実施例1(収斂化粧水) (1) 処方 エタノール 10.0部 柿タンニン(縮合型) 0.5部 クエン酸ナトリウム 0.05部 クエン酸 0.05部 エリソルビン酸 0.4部 エデト酸二ナトリウム 0.1部 ドデシル−β−D−マルトシド 0.4部 香料 0.05部 精製水 88.45部 (2) 製造法Example 1 (astringent lotion) (1) Formulation 10.0 parts of ethanol Persimmon tannin (condensation type) 0.5 part 0.05 parts of sodium citrate 0.05 parts of citric acid 0.4 parts of erythorbic acid 0.4 parts of edet Disodium acid salt 0.1 part Dodecyl-β-D-maltoside 0.4 part Fragrance 0.05 part Purified water 88.45 parts (2) Production method
【0016】上記成分に成分〜を溶解し、この溶
液に成分に成分及び成分を溶解したものを加え、
混合によって均一系にして、本発明の収斂化粧水を得
た。この収斂化粧水を試料として前記諸試験を実施し、
得られた結果を表1に示す。皮膚の収斂作用及び整肌・
保護作用(荒肌改善性)は大変良く、6ケ月間放置後の
外観も沈澱物が生じることなく透明で、化粧料としての
製剤機能を有していた。Ingredients (1) and (2) are dissolved in the above components, and a solution obtained by dissolving the components and components in the components is added to this solution.
The mixture was made uniform to obtain the astringent lotion of the present invention. Performing the above-described tests using this astringent lotion as a sample,
Table 1 shows the obtained results. Astringent action of skin and skin conditioning
The protective action (rough skin improving property) was very good, and the appearance after standing for 6 months was transparent without forming a precipitate, and had a formulation function as a cosmetic.
【0017】[0017]
【表1】 [Table 1]
【0018】比較例1 実施例1に記載の処方成分の代わりにポリオキシエチ
レン(20モル)ソルビタンオレートを用いた他は、同
様の処方及び製造法によって比較例1の収斂化粧水を得
た。これを試料として前記諸試験を実施し、得られた結
果を表1に示す。試料の製造直後、試料に白濁が生じる
と同時に、香料が浮遊ないし分離した。皮膚の収斂作用
が悪く、整肌・保護作用も、やや悪かった。また、6ケ
月間放置後の外観は、2層分離状態を呈し、白濁物も残
存して、化粧料としての製剤機能を失っていた。Comparative Example 1 An astringent lotion of Comparative Example 1 was obtained by the same formulation and production method except that polyoxyethylene (20 mol) sorbitan oleate was used instead of the ingredients described in Example 1. Using these as samples, the above tests were carried out, and the results obtained are shown in Table 1. Immediately after the production of the sample, the sample became cloudy and the fragrance floated or separated. The astringent action of the skin was poor, and the skin conditioning / protective action was somewhat poor. In addition, the appearance after standing for 6 months showed a two-layer separation state, opacity remained, and the formulation function as a cosmetic was lost.
【0019】実施例2(クリーム) (1) 処方 1 スクワラン 25.0部 2 セチルアルコール 3.0部 3 トリ−2−エチルヘキサン酸グリセリン 5.0部 4 デシルグルコシド(β/α=1) 1.0部 5 テトラデシルグルコシド(β/α=1) 1.0部 6 ステアリン酸 0.5部 7 キサンタンガム 0.1部 8 ドデシルマルトシド(β/α=3) 0.7部 9 パラオキシ安息香酸メチル 0.2部 10 エデト酸二ナトリウム 0.1部 11 クエン酸ナトリウム 0.1部 12 L−アスコルビン酸 0.1部 13 タンニン酸(加水分解型) 0.1部 14 香料 0.1部 15 精製水 63.0部 (2) 製造法Example 2 (Cream) (1) Formulation 1 Squalane 25.0 parts 2 Cetyl alcohol 3.0 parts 3 Glycerin tri-2-ethylhexanoate 5.0 parts 4 Decylglucoside (β / α = 1) 1 1.0 part 5 Tetradecyl glucoside (β / α = 1) 1.0 part 6 Stearic acid 0.5 part 7 Xanthan gum 0.1 part 8 Dodecyl maltoside (β / α = 3) 0.7 part 9 Paraoxybenzoic acid Methyl 0.2 part 10 Disodium edetate 0.1 part 11 Sodium citrate 0.1 part 12 L-ascorbic acid 0.1 part 13 Tannic acid (hydrolyzable) 0.1 part 14 Fragrance 0.1 part 15 63.0 parts of purified water (2) Production method
【0020】上記成分1〜5を約80℃にて均一に溶解す
る(溶液I) 。上記成分の水溶性成分7〜9及び15の一
部を約80℃にて均一に溶解する(溶液II)。上記成分15
の残部に10〜13を常温にて均一に溶解する(溶液III
)。次に、溶液Iをホモジナイザーで攪拌しながら、
溶液IIを添加し、乳化した後、冷却する。尚、その冷却
過程の70℃で成分14を添加して30℃まで降温後、溶液II
Iを添加し、攪拌を停止した。このようにして得られた
クリームを試料として前記諸試験を実施し、得られた結
果を表1に示す。皮膚の収斂作用及び整肌・保護作用は
やや良好で、6ケ月間放置後の外観もきめが良く均一
で、化粧料としての製剤機能を有していた。The above components 1 to 5 are uniformly dissolved at about 80 ° C. (solution I). A part of the above water-soluble components 7 to 9 and 15 is uniformly dissolved at about 80 ° C (solution II). Ingredient 15 above
Dissolve 10 to 13 uniformly in the rest of the solution at room temperature (Solution III
). Next, while stirring the solution I with a homogenizer,
Add solution II, emulsify and cool. During the cooling process, component 14 was added at 70 ° C., and after cooling to 30 ° C., the solution II
I was added and stirring was stopped. The creams thus obtained were used as samples to carry out the above-mentioned tests, and the results obtained are shown in Table 1. The astringent action and the skin conditioning / protecting action of the skin were somewhat good, and the appearance after leaving it for 6 months was well-textured and uniform, and had a formulation function as a cosmetic.
【0021】比較例2 実施例2に記載の処方成分の代わりにポリオキシエチ
レン(2モル)セチルエーテルを、成分及びの代わ
りにポリオキシエチレン(20モル)オレイルエーテル
を用いた他は、同様の処方及び製造法によって比較例2
のクリームを得た。これを試料として前記諸試験を実施
し、得られた結果を表1に示す。試料の製造直後の外観
は、クリームのきめが悪く、乳化不良であった。その製
剤の有効性を試験したところ、皮膚の収斂作用は悪く、
整肌・保護作用も悪かった。また、6ケ月間放置後の外
観は、水相と油相が分離し、化粧料としての製剤機能を
失っていた。COMPARATIVE EXAMPLE 2 The same procedure as in Example 2 was repeated except that polyoxyethylene (2 mol) cetyl ether was used in place of the ingredients and polyoxyethylene (20 mol) oleyl ether was used in place of the ingredients. Comparative Example 2 depending on formulation and manufacturing method
I got a cream. Using these as samples, the above tests were carried out, and the results obtained are shown in Table 1. Immediately after the production of the sample, the texture of the cream was poor and the emulsification was poor. When the effectiveness of the formulation was tested, the astringent action of the skin was poor,
Skin conditioning and protection were also poor. In addition, after standing for 6 months, the aqueous phase and the oil phase were separated, and the formulation function as a cosmetic was lost.
【0022】[0022]
【発明の効果】以上記載のごとく、本発明の皮膚化粧料
は、経日安定性が良好で、極めて優れた収斂作用及び整
肌・保護作用を有するものである。As described above, the skin cosmetic composition of the present invention has good stability over time and has an extremely excellent astringent action and skin conditioning / protecting action.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI A61K 7/00 A61K 7/00 W ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI A61K 7/00 A61K 7/00 W
Claims (1)
シドとを含有することを特徴とする皮膚化粧料。1. A skin cosmetic comprising a polyphenol compound and an alkyl glycoside.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP35249691A JP2902842B2 (en) | 1991-12-13 | 1991-12-13 | Skin cosmetics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP35249691A JP2902842B2 (en) | 1991-12-13 | 1991-12-13 | Skin cosmetics |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05163131A JPH05163131A (en) | 1993-06-29 |
JP2902842B2 true JP2902842B2 (en) | 1999-06-07 |
Family
ID=18424473
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP35249691A Expired - Lifetime JP2902842B2 (en) | 1991-12-13 | 1991-12-13 | Skin cosmetics |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2902842B2 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2706478B1 (en) * | 1993-06-14 | 1995-09-08 | Ovi Sa | Compositions of phenolic derivatives, their preparation and their applications as antioxidants. |
JP3515321B2 (en) * | 1997-05-07 | 2004-04-05 | ポーラ化成工業株式会社 | Cosmetic improvement cosmetics |
DE19845271A1 (en) * | 1998-10-01 | 2000-04-06 | Beiersdorf Ag | Cosmetic or dermatological formulation containing flavone, flavanone and/or flavonoid, useful e.g. in skin and hair cosmetics, contains alkylglucoside and optionally alkanol |
KR100367563B1 (en) * | 1998-12-16 | 2003-02-19 | 주식회사 참 존 | Whitening cosmetics containing persimmon leaf extract |
US6685970B1 (en) | 1999-09-21 | 2004-02-03 | Kyowa Hakko Kogyo Co., Ltd. | Compositions containing proanthocyanidin and a vitamin B6 derivative or a salt thereof |
JP4574788B2 (en) | 2000-03-24 | 2010-11-04 | 協和発酵バイオ株式会社 | Proanthocyanidin-containing composition |
US8114829B2 (en) | 2005-02-22 | 2012-02-14 | Human Matrix Sciences, Llc | Elastin protective polyphenolics and methods of using the same |
US8642578B2 (en) | 2005-03-29 | 2014-02-04 | Human Matrix Sciences, Llc | Elastin protective polyphenolics and methods of using the same |
FR2978040B1 (en) * | 2011-07-22 | 2015-01-30 | Oreal | METHOD FOR TREATING HUMAN TRANSPIRATION USING POLYPHENOLS AND CATALYTIC ENZYMATIC AND / OR CHEMICAL OXIDATION SYSTEM |
-
1991
- 1991-12-13 JP JP35249691A patent/JP2902842B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH05163131A (en) | 1993-06-29 |
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