JP3018091B2 - Oily external preparation - Google Patents
Oily external preparationInfo
- Publication number
- JP3018091B2 JP3018091B2 JP2205137A JP20513790A JP3018091B2 JP 3018091 B2 JP3018091 B2 JP 3018091B2 JP 2205137 A JP2205137 A JP 2205137A JP 20513790 A JP20513790 A JP 20513790A JP 3018091 B2 JP3018091 B2 JP 3018091B2
- Authority
- JP
- Japan
- Prior art keywords
- oily
- external preparation
- present
- perfluoropolyether
- weight
- 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.)
- Expired - Fee Related
Links
Landscapes
- Cosmetics (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、油性外用剤に関し、更に詳細には、撥水性
及び耐水性に優れ、かつ耐油性をも有し、汗又は皮脂に
よる薬効成分や顔料等の化粧成分が消失しにくく、さら
に優れた使用感を有する、オイル状パーフルオロポリエ
ーテルをジパーフルオロアルキルリン酸でゲル化させた
油性外用剤に関する。Description: TECHNICAL FIELD The present invention relates to an oily external preparation, and more particularly, to a medicinal component due to sweat or sebum, which has excellent water repellency and water resistance and also has oil resistance. The present invention relates to an oily external preparation obtained by gelling oily perfluoropolyether with diperfluoroalkylphosphoric acid, which makes it difficult for cosmetic components such as pigments and pigments to disappear and has an excellent feeling in use.
固形ないし半固形の油性外用剤は、皮膚に対する付着
力、被覆力、化粧膜の耐水性などの点で優れた特性を有
することから、広く利用されている。従来、このタイプ
の外用剤は、一般に半固体油あるいは液体油及び固体油
からなる油性基剤、又はさらに油性ゲル化剤を配合して
ゲル化させた油性基剤を用い、これに必要に応じて粉体
状の薬効成分や化粧成分を混合、分散させ固化、成型す
ることにより製造されている。Solid or semi-solid oily external preparations are widely used because they have excellent properties such as adhesion to the skin, covering power, and water resistance of the decorative film. Conventionally, this type of external preparation generally uses an oily base composed of a semi-solid oil or a liquid oil and a solid oil, or an oily base mixed with an oily gelling agent and then gelled. It is manufactured by mixing, dispersing, solidifying and molding powdery medicinal and cosmetic ingredients.
しかしながら、これらの油性外用剤は、油分含有量が
多いことから、柔らかくのびを良くしたものは油性感が
極めて強く、また油性感を抑えたものはのびが重くむら
づきするという欠点があり、さらに皮脂によって薬効成
分や顔料等の化粧成分が容易に消失してしまうという問
題もあった。However, since these oily external preparations have a high oil content, those with softness and good spread have a very strong oily feeling, and those with a suppressed oily feeling have the drawback that the spread is heavy and uneven. There is also a problem that cosmetic ingredients such as medicinal ingredients and pigments easily disappear due to sebum.
従って、優れた使用感を有し、しかも耐油性を有し、
皮脂により薬効成分や化粧成分が消失しにくい油性外用
剤が望まれていた。Therefore, it has excellent usability and oil resistance,
There has been a demand for an oily external preparation in which the medicinal and cosmetic ingredients are less likely to disappear due to sebum.
かかる実情において、本発明者らは鋭意研究を行なっ
た結果、オイル状のパーフルオロポリエーテルにジパー
フルオロアルキルリン酸を加えるとゲル化し、これらを
用いれば使用感に優れ、かつ皮脂によって薬効成分や化
粧成分が消失にしくい油性外用剤が得られることを見出
し、本発明を完成した。Under such circumstances, the present inventors have conducted intensive studies and as a result, when diperfluoroalkyl phosphoric acid was added to oily perfluoropolyether, it gelled, and when these were used, the feeling of use was excellent, and the medicinal component was obtained by sebum. The present inventors have found that an oily external preparation that hardly disappears and cosmetic components can be obtained, and completed the present invention.
すなわち、本発明は、成分(A)及び(B) (A)ジパーフルオロアルキルリン酸 0.1〜10重量% (B)オイル状パーフルオロポリエーテル10〜99重量% を含有することを特徴とする油性外用剤を提供するもの
である。That is, the present invention is characterized by containing the components (A) and (B) (A) 0.1 to 10% by weight of diperfluoroalkyl phosphoric acid (B) 10 to 99% by weight of oily perfluoropolyether. An oily external preparation is provided.
本発明で用いられる(A)成分のジパーフルオロアル
キルリン酸としては、例えば次の一般式(I)で表わさ
れるものが挙げられる。Examples of the diperfluoroalkyl phosphoric acid of the component (A) used in the present invention include those represented by the following general formula (I).
〔式中、R1及びR2は炭素数3〜21のパーフルオロアルキ
ル基又はパーフルオロオキシアルキル基を示し、B1及び
B2は2価の架橋基を示し、及びpは0又は1を示し、
m及びqは1〜12の整数を示す〕 一般式(I)において、R1及びR2で示されるパーフル
オロアルキル基としては、直鎖状、分岐状、環状及びこ
れらを組合わせた構造のものが挙げられる。また、例え
ば(CF3)2CFOCF2CF2−などのように炭素原子の間に酸
素原子が挿入したものであってもよい。B1及びB2で示さ
れる2価の架橋基としては、例えば−CO2−,−SO2−,
−O−,−(CH2)3−O−,−S−,−(CH2)m−NR
3−,−CO−NR3−又は−SO2−NR3−(ここで、mは1〜
6の整数を示し、R3は水素原子又は炭素数1〜5のアル
キル基を示す)などが挙げられる。これらの内、R1、R2
が炭素数1〜20のパーフルオロアルキル基であり、=
p=0で、m及びqが1〜5であるジパーフルオロアル
キルリン酸が好ましい。 Wherein R 1 and R 2 represent a perfluoroalkyl group or a perfluorooxyalkyl group having 3 to 21 carbon atoms, and B 1 and
B 2 represents a divalent crosslinking group, and p represents 0 or 1,
m and q each represent an integer of 1 to 12.] In the general formula (I), the perfluoroalkyl group represented by R 1 and R 2 may be a linear, branched, cyclic, or a combination thereof. Things. Further, oxygen atoms may be inserted between carbon atoms, such as (CF 3 ) 2 CFOCF 2 CF 2 —. The divalent bridging group represented by B 1 and B 2, for example, -CO 2 -, - SO 2 - ,
-O -, - (CH 2) 3 -O -, - S -, - (CH 2) m -NR
3- , -CO-NR 3 -or -SO 2 -NR 3- (where m is 1 to
And R 3 represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms). Of these, R 1 , R 2
Is a perfluoroalkyl group having 1 to 20 carbon atoms;
A diperfluoroalkyl phosphoric acid in which p = 0 and m and q are 1 to 5 is preferred.
これらジパーフルオロアルキルリン酸は、一種又は二
種以上を組合わせて用いることができ、全組成中に0.1
〜10重量%(以下、単に%で示す)、好ましくは2〜7
%配合される。These diperfluoroalkyl phosphoric acids can be used alone or in combination of two or more.
To 10% by weight (hereinafter simply referred to as%), preferably 2 to 7%
%.
(B)成分のオイル状パーフルオロポリエーテルとし
ては、例えば次の一般式(II)で表わされるものが挙げ
られる。Examples of the oily perfluoropolyether as the component (B) include those represented by the following general formula (II).
〔式中、R1、R3、R4及びR5は同一でも異なってもよく、
それぞれフッ素原子、パーフルオロアルキル基又はパー
フルオロアルキルオキシ基を、R2はフッ素原子又はパー
フルオロアルキル基を、r、s及びtは分子量が500〜1
00,000となる0以上の数を示す。ただし、r=s=t=
0となることはない。〕 なお、ここでカッコ内に示される各パーフルオロ基は
この順で並んでいる必要はなく、またランダム重合でも
ブロック重合でもかまわない。かかるパーフルオロポリ
エーテルとしては、特に粘度が5〜5,000cStの液体状の
ものが好ましく、例えば次の一般式(III) (式中、x及びyは分子量が500〜10,000となる数を示
し、x/yは0.2〜2である。) で表わされるFOMBLIN HC−04(平均分子量1,500)、同H
C−25(同3,200)及び同HC−R(同6,600)(以上モン
テフロス社製)や、次の一般式(IV) FCF2CF2CF2OzCF2CF3 (IV) (式中、zは4〜500の数を示す。) で表わされるデムナムS−20(重量平均分子量25,00
0)、同S−65(同4,500)、同S−100(同5,600)及び
同S−200(同8,400)(以上ダイキン工業社製)などの
市販品を使用することができる。 Wherein R 1 , R 3 , R 4 and R 5 may be the same or different,
Each of a fluorine atom, a perfluoroalkyl group or a perfluoroalkyloxy group, R 2 represents a fluorine atom or a perfluoroalkyl group, and r, s and t have a molecular weight of 500 to 1
Indicates a number of 0 or more that becomes 00,000. Where r = s = t =
It cannot be zero. The perfluoro groups shown in parentheses need not be arranged in this order, and may be random polymerization or block polymerization. As the perfluoropolyether, a liquid having a viscosity of 5 to 5,000 cSt is particularly preferable. For example, the following general formula (III) (In the formula, x and y are numbers each having a molecular weight of 500 to 10,000, and x / y is 0.2 to 2.) FOMBLIN HC-04 (average molecular weight 1,500), and H
C-25 (the 3,200) and the HC-R (the 6,600) (more Montefurosu Co.) and the following general formula (IV) FCF 2 CF 2 CF 2 O z CF 2 CF 3 (IV) ( in the formula, z represents a number from 4 to 500.) Demnum S-20 (weight average molecular weight 25,000)
0), S-65 (4,500), S-100 (5,600), and S-200 (8,400) (all manufactured by Daikin Industries, Ltd.) can be used.
これらパーフルオロポリエーテルは、全組成中に10〜
99%、好ましくは10〜60%配合される。These perfluoropolyethers have a total composition of 10 to
99%, preferably 10 to 60% is blended.
本発明の外用剤には、前記必須成分のほか、薬効成分
や化粧成分を有効量配合することができる。かかる薬効
成分としては殺菌剤、制汗剤、消炎剤、等が、化粧成分
としては無機又は有機の体質顔料又は着色顔料、紫外線
吸収剤等が挙げられる。The external preparation of the present invention can contain an effective amount of a medicinal component and a cosmetic component in addition to the essential components. Such medicinal components include bactericides, antiperspirants, anti-inflammatory agents, and the like, and cosmetic components include inorganic or organic extenders or coloring pigments, ultraviolet absorbers, and the like.
更に、本発明の外用剤にはこれらの成分の他に、必要
に応じて通常の外用剤に使用される成分、例えばワセリ
ン、ラノリン、セレシン、マイクロクリスタリンワック
ス、カルナバロウ、キャンデリラロウ、高級脂肪酸、高
級アルコール、デキストリン脂肪酸エステル、ショ糖脂
肪酸エステル、コレステロール誘導体等の固形・半固形
油分;スクワラン、流動パラフィン、エステル油、トリ
グリセライド、シリコン油等の流動油分;保湿剤、非イ
オン界面活性剤、水、防腐剤、香料、金属イオン封鎖剤
などを、本発明の効果を損なわない範囲で配合すること
ができる。Further, in addition to these components, the external preparation of the present invention may contain, if necessary, components used in ordinary external preparations, such as petrolatum, lanolin, ceresin, microcrystalline wax, carnauba wax, candelilla wax, higher fatty acids, Solid or semi-solid oils such as higher alcohols, dextrin fatty acid esters, sucrose fatty acid esters, and cholesterol derivatives; liquid oils such as squalane, liquid paraffin, ester oil, triglyceride, and silicone oil; humectants, nonionic surfactants, water, Preservatives, fragrances, sequestering agents and the like can be blended within a range that does not impair the effects of the present invention.
本発明の油性外用剤は、通常の方法に従って製造する
ことができ、油性ファンデーション、ほお紅、油性アイ
シャドウ、油性静菌用クリーム、外用軟膏などとして適
用することができる。The oily external preparation of the present invention can be produced according to a usual method, and can be applied as an oily foundation, blusher, oily eye shadow, oily bacteriostatic cream, topical ointment and the like.
本発明の油性外用剤は、塗布時ののびがなめらかでむ
らづきしない等の優れた使用感を有し、撥水性及び耐水
性にも優れ、しかも耐油性をも有し、汗又は皮脂により
薬効成分や顔料等の化粧成分が消失しにくく、経時での
持続性が良好なものである。The oily external preparation of the present invention has an excellent usability such as smooth and non-smooth spreading at the time of application, excellent water repellency and water resistance, and also has oil resistance, and is efficacious by sweat or sebum. A cosmetic component such as a component or a pigment is hardly lost, and the durability over time is good.
次に実施例を挙げ、本発明を更に説明する。 Next, the present invention will be further described with reference to examples.
製造例1 丸底フラスコ(又はニーダー)に顔料150gを入れ、混
合しながら60℃まで加熱する。これに、(C6F13CH2CH
2O)2P(O)OH13gをイソプロピルエーテル1500gに溶解
加温(50℃)しておいたものを加え、60℃で4時間混合
する。その後、50〜60℃にて、イソプロピルエーテルを
減圧留去し、乾燥してフッ素化合物処理顔料157gを得
た。Production Example 1 150 g of a pigment is placed in a round bottom flask (or kneader) and heated to 60 ° C. while mixing. In addition, (C 6 F 13 CH 2 CH
2 O) 2 P (O) OH13g isopropyl ether 1500g dissolved warmed (50 ° C.) to what had been added and mixed for 4 hours at 60 ° C.. Thereafter, isopropyl ether was distilled off under reduced pressure at 50 to 60 ° C. and dried to obtain 157 g of a fluorine compound-treated pigment.
製造例2 丸底フラスコ(又はニーダー)に(C8F17CH2CH2O)2P
(O)OH17gとイソプロピルアルコール1500gを入れ、60
℃まで加熱溶解し、これに顔料150gを加え、60℃で4時
間混合する。その後、50〜60℃にてイソプロピルアルコ
ールを減圧留去し、乾燥して、フッ素化合物処理顔料16
1gを得た。Production Example 2 (C 8 F 17 CH 2 CH 2 O) 2 P in a round bottom flask (or kneader)
(O) Add 17g of OH and 1500g of isopropyl alcohol, and add
The mixture was heated and melted to 150 ° C., and 150 g of the pigment was added thereto, followed by mixing at 60 ° C. for 4 hours. Thereafter, isopropyl alcohol was distilled off under reduced pressure at 50 to 60 ° C., and dried to obtain a fluorine compound-treated pigment 16.
1 g was obtained.
実施例1 油性ファンデーション: 第1表に示す組成の油性ファンデーションを製造し、
のび、べたつき感、化粧持ち及び安定性について評価し
た。結果を第2表に示す。Example 1 Oily foundation: An oily foundation having the composition shown in Table 1 was produced,
Evaluations were made on stretchability, stickiness, makeup durability and stability. The results are shown in Table 2.
<製 法> 香料以外の全てを配合し、充分攪拌混合した後、加熱
(70℃〜100℃)溶解し、その後香料添加し再度攪拌混
合する。これを金皿に充填し、冷却して油性ファンデー
ションを得る。<Manufacturing method> After blending everything except the fragrance, stirring and mixing well, dissolve by heating (70 ° C to 100 ° C), then add the fragrance and mix again with stirring. This is filled in a metal dish and cooled to obtain an oily foundation.
<評価方法> のび、べたつき感、化粧持ち: 10人の専門パネラーにより官能評価を行ない、次の基
準で示した。 <Evaluation method> Spread, sticky feeling, and long-lasting makeup: Sensory evaluation was conducted by 10 specialized panelists, and the results were shown according to the following criteria.
○・・・・・8人以上良い △・・・・・4人〜7人良い ×・・・・・4人未満良い 安定性: 40℃で1カ月保存後の油状ファンデーションについて
評価した。Good: 8 or more good △: Good for 4 to 7 good ×: Good for less than 4 Stability: The oily foundation after storage at 40 ° C for 1 month was evaluated.
○・・・・・油浮き、分離等の異常を認めない ×・・・・・油浮き、分離等の異常を認める 第2表から明らかなように、本発明の油性ファンデー
ションは、パーフルオロポリエーテルとジパーフルオロ
アルキルリン酸を組合わせて用いることにより、使用感
触が良好で、化粧持ちに優れ、しかも安定なものであっ
た。○ ・ ・ ・ ・ No abnormalities such as oil floating and separation are observed × ・ ・ ・ ・ ・ No abnormalities such as oil floating and separation are observed As is evident from Table 2, the oily foundation of the present invention has a good feeling in use, is excellent in cosmetic durability and is stable by using a combination of perfluoropolyether and diperfluoroalkyl phosphoric acid. Met.
実施例2 ほお紅: 実施例1と同様にして、ほお紅を得た。Example 2 Blush: In the same manner as in Example 1, blush was obtained.
(成 分) (重量%) ジメチルポリシロキサン 3.2 ジトリデカフルオロオクチルリン 酸(一般式(I)中、=p=0、 m=q=2、R1=R2=C6F13) 2.0 パーフルオロポリエーテル (モンテフロス社製、FOMBLIN HC−04) 20.0 ショ糖脂肪酸エステル (第一工業製薬(株)製 シュガーワックスA−10E) 0.5 コメデンプン 0.3 赤色202号 2.8 青色404号 0.2 シリコン処理顔料 タルク 53.0 カオリン 14.0 酸化チタン 4.0 香 料 微量 実施例3 油性アイシャドウ 実施例1と同様にして、油性アイシャドウを得た。(Ingredient) (% by weight) Dimethylpolysiloxane 3.2 Ditridecafluorooctylphosphoric acid (= p = 0, m = q = 2, R 1 = R 2 = C 6 F 13 ) in the general formula (I) 2.0 par Fluoropolyethers (FOMBLIN HC-04, manufactured by Montefros) 20.0 Sucrose fatty acid ester (Sugar wax A-10E, manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.) 0.5 Rice starch 0.3 Red 202 No. 2.8 Blue 404 0.2 Silicon-treated pigment Talc 53.0 Kaolin 14.0 Titanium oxide 4.0 Fragrance trace amount Example 3 Oily eye shadow An oily eye shadow was obtained in the same manner as in Example 1.
(成 分) (重量%) オクタメチルシクロテトラシロキサン 残部 パーフルオロポリエーテル (モンテフロス社製、FOMBLIN HC−04) 45.0 ジヘプタデカフルオロデシルリン酸 (一般式(I)中、=p=0、 m=q=2、R1=R2=C8F17) 4.0 マイクロクリスタリンワックス 7.5 デキストリン脂肪酸エステル (千葉製粉(株)製、レオパールKL) 2.0 フッ素化合物処理顔料(製造例1) 雲母チタン 10.0 タルク 3.0 マイカ 5.5 酸化鉄 10.0 香 料 微量 実施例4 油性静菌用クリーム: 実施例1と同様にして、油性静菌用クリームを得た。(Ingredient) (% by weight) Octamethylcyclotetrasiloxane Remainder Perfluoropolyether (FOMBLIN HC-04, manufactured by Montefros) 45.0 Diheptadecafluorodecyl phosphoric acid (In general formula (I), = p = 0, m = Q = 2, R 1 = R 2 = C 8 F 17 ) 4.0 Microcrystalline wax 7.5 Dextrin fatty acid ester (Leopearl KL, manufactured by Chiba Flour Milling Co., Ltd.) 2.0 Fluorine compound-treated pigment (Production Example 1) Titanium mica 10.0 Talc 3.0 Mica 5.5 Iron oxide 10.0 Fragrance trace amount Example 4 Cream for oily bacteriostatic: In the same manner as in Example 1, a cream for oily bacteriostatic was obtained.
(成 分) (重量%) オクタメチルシクロシロキサン 15.0 デカメチルシクロシロキサン 15.0 パーフルオロポリエーテル (モンテフロス社製、FOMBLIN HC−04) 50.0 ジヘプタデカフルオロデシルリン酸 (一般式(I)中、=p=0、 m=q=2、R1=R2=C8F17) 4.0 水 残量 殺菌剤(イルガサンDP−300) 0.2 グリセリンジイソステアレート 5.0 クエン酸 0.5 クエン酸ナトリウム 1.5 香 料 微量 実施例2〜4で得られた油性外用剤は、使用感触が良
好で、持続性に優れ、しかも安定なものであった。(Ingredient) (% by weight) Octamethylcyclosiloxane 15.0 Decamethylcyclosiloxane 15.0 Perfluoropolyether (FOMBLIN HC-04, manufactured by Montefros) 50.0 Diheptadecafluorodecyl phosphate (In the general formula (I), = p = 0, m = q = 2 , R 1 = R 2 = C 8 F 17) 4.0 water balance fungicides (Irgasan DP-300) 0.2 glycerin diisostearate 5.0 citric acid 0.5 sodium citrate 1.5 perfume trace performed The oily external preparations obtained in Examples 2 to 4 had a good feeling in use, excellent durability, and were stable.
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2205137A JP3018091B2 (en) | 1990-08-03 | 1990-08-03 | Oily external preparation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2205137A JP3018091B2 (en) | 1990-08-03 | 1990-08-03 | Oily external preparation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0491012A JPH0491012A (en) | 1992-03-24 |
| JP3018091B2 true JP3018091B2 (en) | 2000-03-13 |
Family
ID=16502040
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2205137A Expired - Fee Related JP3018091B2 (en) | 1990-08-03 | 1990-08-03 | Oily external preparation |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3018091B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9610634B2 (en) * | 2009-09-17 | 2017-04-04 | Unimatec Co., Ltd. | Emulsion and mold-releasing agent using the same |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0859430A (en) * | 1994-08-29 | 1996-03-05 | Kao Corp | Oily solid cosmetics |
-
1990
- 1990-08-03 JP JP2205137A patent/JP3018091B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9610634B2 (en) * | 2009-09-17 | 2017-04-04 | Unimatec Co., Ltd. | Emulsion and mold-releasing agent using the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0491012A (en) | 1992-03-24 |
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