JPH0624954A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPH0624954A
JPH0624954A JP4181159A JP18115992A JPH0624954A JP H0624954 A JPH0624954 A JP H0624954A JP 4181159 A JP4181159 A JP 4181159A JP 18115992 A JP18115992 A JP 18115992A JP H0624954 A JPH0624954 A JP H0624954A
Authority
JP
Japan
Prior art keywords
urea
water
present
cosmetic
skin irritation
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
JP4181159A
Other languages
Japanese (ja)
Other versions
JP2691662B2 (en
Inventor
Tsuneo Shinpou
恒雄 進邦
Mitsutoshi Kimura
光利 木村
Mitsuharu Masuda
光晴 増田
Yuji Suzuki
裕二 鈴木
Yoshihiro Minematsu
義博 峰松
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP4181159A priority Critical patent/JP2691662B2/en
Publication of JPH0624954A publication Critical patent/JPH0624954A/en
Application granted granted Critical
Publication of JP2691662B2 publication Critical patent/JP2691662B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

(57)【要約】 【構成】 下記成分(A)、(B)及び(C): (A)尿素、(B)丁子、緑茶、葛根、桑白皮、甘草、
オウゴン、アロエ及び橙皮のそれぞれの抽出物から選ば
れる一種又は二種以上、(C)水、を含有する化粧料。 【効果】 角質層の水分保持、角質溶解剥離、抗菌、皮
膚吸収亢進等の作用が長期間にわたって維持され、しか
も皮膚刺激等の副作用をもたらすことがない。
(57) [Summary] [Structure] The following components (A), (B) and (C): (A) urea, (B) clove, green tea, kudzu root, mulberry bark, licorice,
A cosmetic containing (C) water, one or two or more kinds selected from respective extracts of sardine, aloe and orange peel. [Effect] The water retention, keratolytic exfoliation, antibacterial action, skin absorption enhancement, etc. of the stratum corneum are maintained for a long period of time, and side effects such as skin irritation are not brought about.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は化粧料に関し、さらに詳
しくは尿素を安定に配合し得る水含有化粧料に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to cosmetics, and more particularly to a water-containing cosmetic in which urea can be stably mixed.

【0002】[0002]

【従来の技術】一般に、尿素は角質層の水分保持能を向
上させ、さらには角質溶解剥離作用、抗菌作用、皮膚吸
収亢進等の皮膚科学的に重要な薬理作用を有することが
知られており、上記尿素の機能を医薬や化粧料に応用す
る試みが、近年、さかんになされている。
2. Description of the Related Art Generally, urea is known to improve the water-retaining ability of the stratum corneum, and further has dermatologically important pharmacological actions such as keratolytic exfoliation action, antibacterial action, and skin absorption enhancement. In recent years, various attempts have been made to apply the above-mentioned function of urea to medicines and cosmetics.

【0003】尿素含有製剤を製造するには、まず尿素水
溶液を得なければならないが、尿素は、通常、水の存在
により不安定化し、長期間保存すると二酸化炭素とアン
モニアとに分解して上記効力を失なうとともに、水溶液
pHが非生理的範囲にまで上昇する傾向を示す。さらに、
乳化化粧料の場合には、発生するアンモニアが乳化系を
崩壊させ、成分分離をひき起すこともある。
In order to produce a urea-containing preparation, an aqueous urea solution must first be obtained. Urea is usually destabilized by the presence of water and decomposed into carbon dioxide and ammonia when stored for a long period of time, resulting in the above-mentioned efficacy. Loses the aqueous solution
The pH tends to rise to the non-physiological range. further,
In the case of emulsified cosmetics, the generated ammonia may disrupt the emulsified system and cause component separation.

【0004】このような水含有製剤での尿素の分解を抑
制するため、尿素安定化剤、例えば乳酸(特公昭47−
47662号公報)、ヒドロキシルアミン塩酸塩(特公
昭58−22475号公報)、脂肪族ジカルボン酸(特
開昭52−105225号公報)、アラントイン(特開
昭58−48441号公報)、アンモニウム化合物(特
開昭59−87035号公報)、中性アミノ酸、酸性ア
ミノ酸又はアミノ酸アルカリ塩(特開昭59−1347
72号公報)等を添加する方法が報告されている。
In order to suppress the decomposition of urea in such a water-containing preparation, a urea stabilizer such as lactic acid (Japanese Patent Publication No. 47-
47662), hydroxylamine hydrochloride (JP-B-58-22475), aliphatic dicarboxylic acid (JP-A-52-105225), allantoin (JP-A-58-48441), ammonium compound (patent JP-A-59-87035), neutral amino acids, acidic amino acids or amino acid alkali salts (JP-A-59-1347).
No. 72) has been reported.

【0005】[0005]

【発明が解決しようとする課題】しかしながら、上記従
来の尿素安定化剤は、いずれもある程度の効果は有する
ものの、数ケ月にわたる長期保存で十分な効果をもたら
すに足るものではない。そこで、皮膚等への刺激を発生
させることなく、長期保存に耐え得る尿素安定化剤を配
合した化粧料の開発が望まれていた。
However, although the above-mentioned conventional urea stabilizers have some effects, they are not sufficient to provide sufficient effects after long-term storage for several months. Therefore, it has been desired to develop a cosmetic containing a urea stabilizer that can withstand long-term storage without causing irritation to the skin or the like.

【0006】[0006]

【課題を解決するための手段】本発明者らは、かかる実
情に鑑み鋭意検討した結果、尿素配合化粧料が、特定の
植物抽出物の添加により、従来にない安定性と皮膚への
安全性をもたらすことを見出し、本発明を完成するに至
った。
[Means for Solving the Problems] The inventors of the present invention have conducted extensive studies in view of the above-mentioned circumstances, and as a result, urea-containing cosmetics have unprecedented stability and safety to the skin due to the addition of a specific plant extract. The present invention has been completed and the present invention has been completed.

【0007】すなわち、本発明は、下記成分(A)、
(B)及び(C): (A)尿素、(B)丁子、緑茶、葛根、桑白皮、甘草、
オウゴン、アロエ及び橙皮のそれぞれの抽出物から選ば
れる一種又は二種以上、(C)水、を含有することを特
徴とする化粧料を提供するものである。
That is, the present invention provides the following component (A),
(B) and (C): (A) urea, (B) clove, green tea, kudzu root, mulberry bark, licorice,
It is intended to provide a cosmetic characterized by containing (C) water, one or more kinds selected from respective extracts of sardine, aloe and orange peel.

【0008】本発明に使用される成分(A)の尿素の本
発明化粧料への配合量は特に限定されないが、0.05
〜10.0重量%(以下単に%という)が好ましい。
0.05%未満では十分な作用が得られず、10%を超
えても効果の増大は殆んどみられない。
The blending amount of urea of the component (A) used in the present invention in the cosmetic of the present invention is not particularly limited, but is 0.05.
-10.0 wt% (hereinafter simply referred to as%) is preferable.
If it is less than 0.05%, a sufficient action cannot be obtained, and if it exceeds 10%, the effect is hardly increased.

【0009】本発明に使用される成分(B)の植物抽出
物は、上記それぞれの植物を水、メタノール、エタノー
ル、1,3−ブチレングリコール、プロピレングリコー
ル等の親水性有機溶媒若しくはこれらの混合溶媒で抽出
して得られる液状物又は該液状物を乾燥して得られる粉
末である。例えば、丁子の抽出物を得るには、丁子のつ
ぼみを乾燥して細切し、これに水/エタノール混合液を
加え、時々攪拌した後室温にて浸漬し、圧搾分離して抽
出液を得た後濾過すればよい。
The plant extract of the component (B) used in the present invention is obtained by treating each of the above plants with a hydrophilic organic solvent such as water, methanol, ethanol, 1,3-butylene glycol or propylene glycol, or a mixed solvent thereof. And a powder obtained by drying the liquid substance obtained by extracting the liquid substance. For example, to obtain a clove extract, the clove buds are dried and finely chopped, a water / ethanol mixed solution is added to this, and the mixture is stirred at room temperature for immersion and squeezed to obtain an extract. Then, it may be filtered.

【0010】成分(B)の植物抽出物の市販品として
は、例えばファルコレックス チョウジ、緑茶リキッ
ド、カッコンエキスパウダー、ファルコレックス ソウ
ハクヒ、オウゴンエキスパウダー、オウゴンリキッド
B、オウゴンリキッドE、オウゴンリキッドSE(以
上、一丸ファルコス(株)製)等が挙げられる。
Examples of commercially available plant extracts of the component (B) include Falco Rex Clove, green tea liquid, cucumber extract powder, Falco Rex Sawakuhi, Ougon extract powder, Ougon Liquid B, Ougon Liquid E, Ougon Liquid SE (above). , Ichimaru Falcos Co., Ltd.) and the like.

【0011】成分(B)は、本発明化粧料中に固形分と
して0.001〜20%、特に0.005〜10%配合
することが好ましい。
The component (B) is preferably added in the cosmetic of the present invention in a solid content of 0.001 to 20%, particularly 0.005 to 10%.

【0012】本発明に使用される成分(C)の水は精製
水であることが好ましい。配合量はとくに限定されず、
各種化粧料への配合可能量であればよい。
The component (C) water used in the present invention is preferably purified water. The blending amount is not particularly limited,
Any amount can be used as long as it can be added to various cosmetics.

【0013】本発明化粧料の水相pHはとくに限定されな
いが、非生理的pH範囲では皮膚刺激が発生することがあ
り好ましくない。好ましいpH範囲は5.0〜8.0であ
る。
The pH of the aqueous phase of the cosmetic composition of the present invention is not particularly limited, but skin irritation may occur in a non-physiological pH range, which is not preferable. The preferred pH range is 5.0 to 8.0.

【0014】尿素含有水溶液のpHを安定させるための緩
衝系としては、特に限定されないが、例えばリン酸緩衝
系、クエン酸緩衝系、リン酸−クエン酸緩衝系等が挙げ
られる。
The buffer system for stabilizing the pH of the urea-containing aqueous solution is not particularly limited, and examples thereof include a phosphate buffer system, a citrate buffer system, and a phosphate-citrate buffer system.

【0015】本発明の化粧料には、本発明の効果を損な
わない範囲において、上記必須成分以外の通常化粧品、
医薬部外品、医薬品等に用いられる各種任意成分を適宜
配合することができる。かかる任意成分としては、例え
ばエタノール、油性物質、保湿剤、増粘剤、防腐剤、乳
化剤、薬効成分、粉体、紫外線吸収剤、色素、香料、乳
化安定剤等を挙げることができる。
The cosmetics of the present invention include ordinary cosmetics other than the above-mentioned essential components as long as the effects of the present invention are not impaired.
Various optional ingredients used in quasi-drugs, pharmaceuticals and the like can be appropriately mixed. Examples of such optional components include ethanol, oily substances, moisturizers, thickeners, preservatives, emulsifiers, medicinal components, powders, ultraviolet absorbers, dyes, fragrances, and emulsion stabilizers.

【0016】具体的には、油性成分として流動パラフィ
ン、ワセリン、パラフィンワックス、スクワラン、ミツ
ロウ、カルナウバロウ、オリーブ油、ラノリン、高級ア
ルコール脂肪酸、高級アルコールと脂肪酸の合成エステ
ル油、シリコーン油等が挙げられ、保湿剤としてはソル
ビトール、キシリトール、グリセリン、マルチトール、
プロピレングリコール、1,3−ブチレングリコール、
1,4−ブチレングリコール、ピリドンカルボン酸ナト
リウム、乳酸、乳酸ナトリウム、ポリオキシプロピレン
脂肪酸エステル、ポリエチレングリコール等が挙げら
れ、増粘剤としてはカルボキシビニルポリマー、カルボ
キシメチルセルロース、ポリビニルアルコール、カラギ
ーナン、ゼラチン等の水溶性高分子、塩化ナトリウム、
塩化カリウム等の電解質などが挙げられ、防腐剤として
はメチルパラベン、エチルパラベン、プロピルパラベ
ン、ブチルパラベン、安息香酸ナトリウム等が挙げら
れ、乳化剤としてはポリオキシエチレンアルキルエーテ
ル、ポリオキシエチレン脂肪酸エステル、ポリグリセリ
ン脂肪酸エステル、ポリオキシエチレングリセリン脂肪
酸エステル、ポリオキシエチレン硬化ヒマシ油、ポリオ
キシエチレンソルビトール脂肪酸エステル等の非イオン
界面活性剤が挙げられ、粉体としてはタルク、セリサイ
ト、マイカ、カオリン、シリカ、ベントナイト、バーミ
キュライト、亜鉛華、雲母、雲母チタン、酸化マグネシ
ウム、酸化ジルコニウム、硫酸バリウム、ベンガラ、酸
化鉄、群青等が挙げられる。
Specific examples of the oily component include liquid paraffin, petrolatum, paraffin wax, squalane, beeswax, carnauba wax, olive oil, lanolin, higher alcohol fatty acids, synthetic ester oils of higher alcohols and fatty acids, silicone oils, etc. As agents, sorbitol, xylitol, glycerin, maltitol,
Propylene glycol, 1,3-butylene glycol,
1,4-butylene glycol, sodium pyridonecarboxylate, lactic acid, sodium lactate, polyoxypropylene fatty acid ester, polyethylene glycol and the like can be mentioned. Thickeners include carboxyvinyl polymer, carboxymethyl cellulose, polyvinyl alcohol, carrageenan, gelatin and the like. Water-soluble polymer, sodium chloride,
Examples include electrolytes such as potassium chloride, preservatives such as methylparaben, ethylparaben, propylparaben, butylparaben, sodium benzoate, etc., and emulsifiers such as polyoxyethylene alkyl ether, polyoxyethylene fatty acid ester, and polyglycerin. Nonionic surfactants such as fatty acid ester, polyoxyethylene glycerin fatty acid ester, polyoxyethylene hydrogenated castor oil, polyoxyethylene sorbitol fatty acid ester, etc. are mentioned, and powders include talc, sericite, mica, kaolin, silica, bentonite. , Vermiculite, zinc white, mica, mica titanium, magnesium oxide, zirconium oxide, barium sulfate, red iron oxide, iron oxide, ultramarine and the like.

【0017】本発明が対象とする化粧料は、一般の皮膚
化粧料に限定されるものではなく、医薬部外品、外用医
薬品等を包含するものであり、その剤型もその目的に応
じて任意に選択することができ、クリーム状、軟膏状、
乳液状、ローション状、溶液状、ゲル状、パック状、ス
ティック状等とすることができる。なかでも、本発明化
粧料は顔用の化粧料であることが好ましい。
The cosmetics to which the present invention is applied are not limited to general skin cosmetics, but include quasi-drugs, external medicines, etc., and their dosage forms are also selected according to the purpose. Can be selected arbitrarily, creamy, ointment,
It can be in the form of emulsion, lotion, solution, gel, pack, stick or the like. Among them, the cosmetic of the present invention is preferably a facial cosmetic.

【0018】本発明の化粧料は、常法に従い製造するこ
とができる。
The cosmetic composition of the present invention can be manufactured by a conventional method.

【0019】[0019]

【発明の効果】本発明化粧料は、その成分である尿素が
長期間にわたり、きわめて安定に存在することから、そ
の良好な生理作用、角質層の水分保持、角質溶解剥離、
抗菌、皮膚吸収亢進等が維持され、しかも皮膚刺激等の
副作用をもたらすことがないものであり、各種化粧料に
応用できる。
EFFECTS OF THE INVENTION In the cosmetic of the present invention, urea, which is a component of the cosmetic, is extremely stable over a long period of time, so that its good physiological action, water retention in the stratum corneum, keratolytic peeling,
It has antibacterial properties, enhanced skin absorption, etc., and does not cause side effects such as skin irritation, and can be applied to various cosmetics.

【0020】[0020]

【実施例】以下に本発明を実施例により具体的に説明す
るが、本発明はこれらに限定されるものではない。
EXAMPLES The present invention will be described in detail below with reference to examples, but the present invention is not limited thereto.

【0021】実施例1 以下に組成を示すエモリエントクリームを下記方法によ
り製造した。
Example 1 An emollient cream having the following composition was produced by the following method.

【0022】[0022]

【表1】 (重量%) 油相成分: (1)ワセリン 6.0 (2)スクワラン 33.5 (3)セタノール 4.0 (4)ホホバ油 5.0 (5)モノ脂肪酸グリセリン 2.0 (6)P.O.E.(20)ソルビタンモノラウリン酸エステル 2.0 (7)メチルパラベン 0.2 水相成分: (8)グリセリン 15.0 (9)尿素 5.0 (10)安定化剤 表2に示す種類及び量 (11)精製水 残余(Table 1) (wt%) Oil phase components: (1) Vaseline 6.0 (2) Squalane 33.5 (3) Cetanol 4.0 (4) Jojoba oil 5.0 (5) Mono-fatty acid glycerin 2.0 (6) POE (20) sorbitan monolaurate 2.0 (7) Methylparaben 0.2 Aqueous phase component: (8) Glycerin 15.0 (9) Urea 5.0 (10) Stabilizer Types shown in Table 2 And quantity (11) Purified water Residual

【0023】(製造方法)上記油相成分を混合し、加熱
溶解して70℃にする。一方、上記水相成分を加熱して
50℃に保つ。この水相部に油相部を加えて乳化機にて
乳化する。乳化物を熱交換機にて終温30℃まで冷却し
た後、充填する。
(Manufacturing Method) The above oil phase components are mixed and heated to melt to 70 ° C. On the other hand, the aqueous phase component is heated and kept at 50 ° C. The oil phase part is added to this water phase part and emulsified by an emulsifying machine. The emulsion is cooled to a final temperature of 30 ° C. by a heat exchanger and then filled.

【0024】得られたエモリエントクリームを40℃に
て保存し、経日によるアンモニア臭の有無及び皮膚刺激
性(ヒリヒリ感)を下記基準により専門パネリスト10
名が官能評価した。結果(平均値)を併せて表2に示
す。
The obtained emollient cream was stored at 40 ° C., and the presence or absence of ammonia odor due to aging and the skin irritation (irritating sensation) were determined according to the following criteria.
The name was sensory evaluated. The results (average value) are also shown in Table 2.

【0025】(評価基準) アンモニア臭:○;アンモニア臭なし、 △;アンモニア臭ややあり、 ×;アンモニア臭あり、 皮膚刺激性:○;皮膚刺激性なし、 △;皮膚刺激性ややあり、 ×;皮膚刺激性あり、(Evaluation Criteria) Ammonia odor: ◯: No ammonia odor, Δ: Slight ammonia odor, ×: Ammonia odor, Skin irritation: ◯: No skin irritation, Δ: Some skin irritation, ×; Skin irritation,

【0026】[0026]

【表2】 [Table 2]

【0027】表2に示すように、本発明のエモリエント
クリームは、長期間にわたってアンモニア臭がなく、か
つ皮膚刺激性を示さないという良好な性質を有するもの
であった。一方、従来の安定化剤を使用した比較例にお
いては経日によるアンモニア臭及び皮膚刺激の増加が大
であった。
As shown in Table 2, the emollient cream of the present invention had good properties such as no odor of ammonia and no skin irritation over a long period of time. On the other hand, in the comparative example using the conventional stabilizer, the increase in ammonia odor and skin irritation with the passage of time was large.

【0028】実施例2 以下に組成を示す化粧水を下記方法により製造した。Example 2 A lotion having the following composition was produced by the following method.

【0029】[0029]

【表3】 (重量%) (1)エタノール 15.0 (2)グリセリン 5.0 (3)ポリエチレングリコール1500 2.0 (4)P.O.E.(20)オレイルエーテル 2.0 (5)メチルパラベン 0.2 (6)尿素 5.0 (7)植物抽出物 表4に示す種類及び量 (8)精製水 残余(Table 3) (% by weight) (1) Ethanol 15.0 (2) Glycerin 5.0 (3) Polyethylene glycol 1500 2.0 (4) POE (20) Oleyl ether 2.0 (5) Methylparaben 0.2 (6) Urea 5.0 (7) Plant extract Types and amounts shown in Table 4 (8) Purified water Residue

【0030】(製造方法)精製水に(2)、(3)、
(6)及び(7)を加え、室温下で溶解する。一方、エ
タノールに(4)及び(5)を加え同じく室温下で溶解
した後、水相に加えて可溶化し、濾過した後充填した。
(Production method) In purified water, (2), (3),
Add (6) and (7) and dissolve at room temperature. On the other hand, after adding (4) and (5) to ethanol and dissolving them at room temperature in the same manner, they were added to the aqueous phase to be solubilized, filtered, and then filled.

【0031】得られた化粧水を40℃にて120日間保
存後、実施例1と同様の評価を行なった。結果を併せて
表4に示す。
The lotion thus obtained was stored at 40 ° C. for 120 days and then evaluated in the same manner as in Example 1. The results are also shown in Table 4.

【0032】[0032]

【表4】 [Table 4]

【0033】表4に示すように、本発明の化粧水は長期
間にわたってアンモニア臭がなく、かつ皮膚刺激性を示
さないという良好な性質を有するものであった。
As shown in Table 4, the lotion of the present invention had good properties such as no odor of ammonia and no skin irritation for a long period of time.

【0034】実施例3 以下に組成を示すエモリエントローションを下記の方法
により製造した。
Example 3 An emollient lotion having the following composition was produced by the following method.

【0035】[0035]

【表5】 (重量%) 油相成分: (1)セタノール 1.0 (2)スクワラン 5.0 (3)ワセリン 2.0 (4)ラノリンアルコール 0.5 (5)ステアリン酸 2.0 (6)P.O.E.(20)ソルビタンモノラウリン酸エステル 2.0 水相成分: (7)グリセリン 3.0 (8)プロピレングリコール 3.0 (9)トリエタノールアミン 1.0 (10)尿素 5.0 (11)植物抽出物 表6に示す種類及び量 (12)精製水 残余(Table 5) (wt%) Oil phase component: (1) Cetanol 1.0 (2) Squalane 5.0 (3) Vaseline 2.0 (4) Lanolin alcohol 0.5 (5) Stearic acid 2.0 ( 6) POE (20) sorbitan monolaurate 2.0 Water phase components: (7) Glycerin 3.0 (8) Propylene glycol 3.0 (9) Triethanolamine 1.0 (10) Urea 5.0 (11 ) Plant extract Types and amounts shown in Table 6 (12) Purified water Residue

【0036】(製造方法)油相成分を混合し加熱溶解し
て70℃に保つ。上記水相成分も50℃で同様に加熱混
合し、この水相部に前述の油相部を加えて、乳化機にて
乳化する。乳化物を30℃まで冷却した後、充填した。
(Manufacturing Method) The oil phase components are mixed, heated and dissolved, and maintained at 70 ° C. Similarly, the above water phase components are heated and mixed at 50 ° C., the above oil phase part is added to this water phase part, and the mixture is emulsified by an emulsifying machine. The emulsion was cooled to 30 ° C. and then filled.

【0037】得られたエモリエントローションを40℃
にて120日間保存後、実施例1と同様の評価を行なっ
た。結果を併せて表6に示す。
The obtained emollient lotion was treated at 40 ° C.
After 120 days of storage, the same evaluation as in Example 1 was performed. The results are also shown in Table 6.

【0038】[0038]

【表6】 [Table 6]

【0039】表6に示すように、本発明のエモリエント
ローションは長期間にわたってアンモニア臭がなく、か
つ皮膚刺激性を示さないという良好な性質を有するもの
であった。
As shown in Table 6, the emollient lotion of the present invention had good properties such as no odor of ammonia for a long period of time and no skin irritation.

【0040】実施例4 以下に組成を示す美白クリームを下記方法により製造し
た。
Example 4 A whitening cream having the following composition was produced by the following method.

【0041】[0041]

【表7】 (重量%) 油相成分: (1)ステアリン酸デカグリセリル 1.8 (2)ポリオキシエチレンセチルエーテル 1.2 (3)スクワラン 12.0 (4)セタノール 6.0 (5)パルミチン酸セチル 3.0 水相成分: (6)1,3−ブチレングリコール 6.0 (7)グリセリン 3.0 (8)エデト酸4ナトリウム 0.1 (9)L−アスコルビン酸リン酸エステルマグネシウム塩 3.0 (10)植物抽出物 表8に示す種類及び量 (11)尿素 5.0 (12)クエン酸ナトリウム 1.0 (13)精製水 残余(Table 7) (wt%) Oil phase component: (1) Decaglyceryl stearate 1.8 (2) Polyoxyethylene cetyl ether 1.2 (3) Squalane 12.0 (4) Cetanol 6.0 (5) Cetyl palmitate 3.0 Aqueous phase component: (6) 1,3-butylene glycol 6.0 (7) Glycerin 3.0 (8) Edetate 4 sodium 0.1 (9) L-ascorbic acid phosphate magnesium ester Salt 3.0 (10) Plant extract Type and amount shown in Table 8 (11) Urea 5.0 (12) Sodium citrate 1.0 (13) Purified water Residue

【0042】(製造方法)油相成分を混合し加熱溶解し
て70℃に保つ。上記水相成分も50℃で同様に加熱混
合し、この水相部に前述の油相部を加えて、乳化機にて
乳化する。乳化物を30℃まで冷却した後、充填する。
(Manufacturing method) The oil phase components are mixed, heated and dissolved, and maintained at 70 ° C. Similarly, the above water phase components are heated and mixed at 50 ° C., the above oil phase part is added to this water phase part, and the mixture is emulsified by an emulsifying machine. The emulsion is cooled to 30 ° C. and then filled.

【0043】得られた美白クリームを40℃にて120
日間保存後、実施例1と同様の評価を行なった。結果を
併せて表8に示す。
The whitening cream obtained is treated at 120 ° C. for 120 minutes.
After storage for a day, the same evaluation as in Example 1 was performed. The results are also shown in Table 8.

【0044】[0044]

【表8】 [Table 8]

【0045】表8に示すように、本発明の美白クリーム
は、長期間にわたってアンモニア臭がなく、かつ皮膚刺
激性を示さないという良好な性質を有するものであっ
た。
As shown in Table 8, the whitening cream of the present invention had good properties such as no smell of ammonia and no skin irritation for a long period of time.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 峰松 義博 アメリカ合衆国 オハイオ州 シンシナチ コートブルック ビレッジ 11424 ─────────────────────────────────────────────────── ─── Continued Front Page (72) Inventor Yoshihiro Minematsu 11424, Cincinnati Courtbrook Village, Ohio, United States 11424

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 下記成分(A)、(B)及び(C): (A)尿素、(B)丁字、緑茶、葛根、桑白皮、甘草、
オウゴン、アロエ及び橙皮のそれぞれの抽出物から選ば
れる一種又は二種以上、(C)水、を含有することを特
徴とする化粧料。
1. The following components (A), (B) and (C): (A) urea, (B) Dingji, green tea, kudzu root, mulberry bark, licorice,
A cosmetic comprising (C) water, one or more kinds selected from respective extracts of sardine, aloe and orange peel.
JP4181159A 1992-07-08 1992-07-08 Cosmetics Expired - Lifetime JP2691662B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4181159A JP2691662B2 (en) 1992-07-08 1992-07-08 Cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4181159A JP2691662B2 (en) 1992-07-08 1992-07-08 Cosmetics

Publications (2)

Publication Number Publication Date
JPH0624954A true JPH0624954A (en) 1994-02-01
JP2691662B2 JP2691662B2 (en) 1997-12-17

Family

ID=16095921

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4181159A Expired - Lifetime JP2691662B2 (en) 1992-07-08 1992-07-08 Cosmetics

Country Status (1)

Country Link
JP (1) JP2691662B2 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0920630A (en) * 1995-07-06 1997-01-21 Nippon Zetotsuku Kk Cosmetic material
JPH09255519A (en) * 1996-03-19 1997-09-30 Noevir Co Ltd Antibacterial low irritating cosmetic material
FR2747884A1 (en) * 1996-04-26 1997-10-31 Haitai Confectionery Company L Extract derived from clove bark and flower stems
US6248341B1 (en) 2000-01-14 2001-06-19 Color Access, Inc. Method of treating topical angiogenesis-related disorders
KR100516447B1 (en) * 1997-11-20 2005-12-06 주식회사 엘지생활건강 Cosmetic composition containing root extract with excellent astringent effect
JP2009298748A (en) * 2008-06-17 2009-12-24 Septem Soken:Kk Liquid crystal lamellar type composition for cosmetic and cosmetic containing the same
CN102526391A (en) * 2010-12-16 2012-07-04 天津中敖生物科技有限公司 Livestock Chinese medicinal composition with refrigerating function and preparation method thereof
JP2012224637A (en) * 2002-11-19 2012-11-15 Basf Beauty Care Solutions France Sas Method of testing activity of potentially active substance to inhibit enzymatic activity of phospholipase a2
US10500168B2 (en) * 2003-11-10 2019-12-10 Beiersdorf Ag Use of licochalcone a for treatment of rosacea

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0920630A (en) * 1995-07-06 1997-01-21 Nippon Zetotsuku Kk Cosmetic material
JPH09255519A (en) * 1996-03-19 1997-09-30 Noevir Co Ltd Antibacterial low irritating cosmetic material
FR2747884A1 (en) * 1996-04-26 1997-10-31 Haitai Confectionery Company L Extract derived from clove bark and flower stems
KR100516447B1 (en) * 1997-11-20 2005-12-06 주식회사 엘지생활건강 Cosmetic composition containing root extract with excellent astringent effect
US6248341B1 (en) 2000-01-14 2001-06-19 Color Access, Inc. Method of treating topical angiogenesis-related disorders
JP2012224637A (en) * 2002-11-19 2012-11-15 Basf Beauty Care Solutions France Sas Method of testing activity of potentially active substance to inhibit enzymatic activity of phospholipase a2
US10500168B2 (en) * 2003-11-10 2019-12-10 Beiersdorf Ag Use of licochalcone a for treatment of rosacea
JP2009298748A (en) * 2008-06-17 2009-12-24 Septem Soken:Kk Liquid crystal lamellar type composition for cosmetic and cosmetic containing the same
CN102526391A (en) * 2010-12-16 2012-07-04 天津中敖生物科技有限公司 Livestock Chinese medicinal composition with refrigerating function and preparation method thereof

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