JPS6393707A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPS6393707A
JPS6393707A JP24108086A JP24108086A JPS6393707A JP S6393707 A JPS6393707 A JP S6393707A JP 24108086 A JP24108086 A JP 24108086A JP 24108086 A JP24108086 A JP 24108086A JP S6393707 A JPS6393707 A JP S6393707A
Authority
JP
Japan
Prior art keywords
oxide
powder
mica
coating
titanium
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
JP24108086A
Other languages
Japanese (ja)
Inventor
Masuo Hosokawa
益男 細川
Keiichirou Yukimitsu
敬一郎 幸光
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.)
Hosokawa Micron Corp
Original Assignee
Hosokawa Micron 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 Hosokawa Micron Corp filed Critical Hosokawa Micron Corp
Priority to JP24108086A priority Critical patent/JPS6393707A/en
Publication of JPS6393707A publication Critical patent/JPS6393707A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/11Encapsulated compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/41Particular ingredients further characterized by their size
    • A61K2800/412Microsized, i.e. having sizes between 0.1 and 100 microns

Abstract

PURPOSE:To produce a cosmetic having excellent hydrophilic nature and surface gloss and capable of giving smooth feeling and good spreadability to the skin, by bonding inorganic powder in the form of spheres and coating the surface with ultrafine powder only by mixing and stirring. CONSTITUTION:One ore more kinds of inorganic powder such as silica, calcium silicate, aluminum silicate, bentonite, mica, titanium mica, etc., are bonded to form a sphere and the surface of the obtained spherical core substance is coated with another ultramicro-pulverized powder (e.g. inorganic powder such as silica, titanium oxide, talc, etc., resin, pigment, gold, copper, etc.) only by mixing and stirring absolutely without using a bonding agent such as binder. The particle diameter of the core substance is preferably about 0.1-30mu and that of the ultrafine powder for coating is preferably 0.005-5mu.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、親水性と表面光沢性に優れ、感触的になめら
かさと伸びのよさを与えるように核となる球状芯物質に
対し、別途微粉末を表面にコーティングさせて生成した
化粧料に関する。
[Detailed Description of the Invention] [Industrial Field of Application] The present invention is characterized by the fact that the spherical core material, which is the core, has a finely divided material that has excellent hydrophilicity and surface gloss, and provides smoothness and stretchability to the touch. This invention relates to cosmetics produced by coating the surface with powder.

〔従来技術〕[Prior art]

従来、化粧料として芯物質表面に別の微粉末をコーティ
ングさせるものでは芯となる母材に熱可塑性樹脂を用い
、これに金属、金属酸化物、金属化合物、顔料その他の
微粉末をコーティングさせていた。例としては、特開昭
61−194010号公報がある。
Conventionally, cosmetics in which the surface of a core substance is coated with another fine powder use a thermoplastic resin as the core base material, which is then coated with metals, metal oxides, metal compounds, pigments, and other fine powders. Ta. An example is JP-A-61-194010.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

熱可塑性樹脂は粒径が平均30ミクロンと粗く、粒度分
布の巾も広いなど均一で安定した製品を得難く、化粧料
としては十分なものではなかった。又、熱可塑性樹脂を
母材とし、その表面に金属や顔料、その他の微粉末をコ
ーティングさせる場合、通常母材とコーティング用微粉
末のほかに結合剤としてバインダーを添加するのが一般
的である。但し、このバインダーは相当な熱が加わると
溶融し、コーティングされた微粉末が剥離され易いこと
Thermoplastic resins have a coarse particle size of 30 microns on average, and have a wide particle size distribution, making it difficult to obtain uniform and stable products, making them unsuitable for use as cosmetics. Furthermore, when a thermoplastic resin is used as a base material and its surface is coated with metal, pigment, or other fine powder, it is common to add a binder as a binder in addition to the base material and the fine coating powder. . However, this binder melts when a considerable amount of heat is applied, and the coated fine powder is likely to peel off.

又、ホリエチレンの球状粒子は、熱が加わるとその熱に
より溶融する事があり、使用が制限され、又、PMMA
の球状粒子はアルコール等の溶剤に弱い事からその用途
に制限を受けるものでありjこ。
In addition, polyethylene spherical particles may melt when heated, which limits their use, and PMMA
The spherical particles are susceptible to solvents such as alcohol, so their uses are limited.

本発明は、このような点に鑑み熱変化がなく、溶剤等耐
薬品性にもすぐれ、均一で安定した化粧料を提供するも
のである。
In view of these points, the present invention provides a uniform and stable cosmetic that does not undergo thermal changes, has excellent resistance to chemicals such as solvents.

C問題を解決するための手段〕 本願は熱可塑性樹脂に替えて無機粉末を一又は複数種結
合させて球状化し、その表面に超微粒子化した微粉末を
一又は複数種バインダー等結合剤を一切使用しないで混
合と攪拌によりコーティングさせたものである。
Means for Solving Problem C] The present application combines one or more kinds of inorganic powders instead of thermoplastic resins to form spherules, and then coats one or more kinds of ultrafine powders on the surface without using any binders such as binders. It is coated by mixing and stirring without using it.

〔作用〕[Effect]

無機粉末を結合し粒径0.1〜30ミクロンに球状化さ
せたものと、粒径0.005〜5ミクロンに超微粒子化
させたコーティング用微粉末とを混合し、攪拌作用を付
加することにより球状化した無機粉末を母材としてその
表面にコーティング用微粉末の強固なコーティング層を
形成させる。すなわち、混合と攪拌の作用によって無機
粉末法と超微粒子化されたコーティング用微粉末とは両
粒子間に働く分子間力と静電気による結合のほか、無機
粉末法の表面に無数に形成された細孔による吸着作用に
よっても母材表面へのコーティング用微粉末の凝集が促
進される。又、コーテイング材として樹脂等融点の低い
微粉末の場合、混合攪拌されることによって無機粉末法
及びコーティング用の樹脂微粉末粒子相方の表面温度が
上昇されることになり、熱暑こよる活性化と共に樹脂微
粉末は溶融状態となり、母材の無機粉末球表面に溶着さ
れてコーティング層を形成させる。化粧料としては、さ
らに油脂、顔料、香料等を添加混合させた後、必要によ
り粒度調整を行い製品とする。
Mixing an inorganic powder that has been spheroidized to a particle size of 0.1 to 30 microns and a coating fine powder that has been ultrafinely pulverized to a particle size of 0.005 to 5 microns, and adding a stirring action to the mixture. Using the spheroidized inorganic powder as a base material, a strong coating layer of fine coating powder is formed on the surface of the base material. In other words, the inorganic powder method and the fine coating powder made into ultra-fine particles by the action of mixing and stirring are combined with the intermolecular force and electrostatic bond between the two particles, as well as the innumerable fine particles formed on the surface of the inorganic powder method. The adsorption effect of the pores also promotes agglomeration of the coating fine powder onto the surface of the base material. In addition, in the case of a fine powder with a low melting point, such as a resin, as a coating material, the surface temperature of the resin fine powder particle partner for inorganic powder method and coating will be increased by mixing and stirring, and activation due to heat and heat will increase. At the same time, the fine resin powder becomes molten and is welded to the surface of the inorganic powder sphere of the base material to form a coating layer. For cosmetics, oils, fats, pigments, fragrances, etc. are further added and mixed, and then the particle size is adjusted as necessary to produce a product.

〔発明の効果〕〔Effect of the invention〕

超微粒子化したコーティング用微粉末を無機粉末法にコ
ーティングさせた化粧料は、以下の点ですぐれた性質を
もっている。すなわち、色彩、光沢が良好、紫外線カツ
ト効果も良好、伸びも良好、他の化粧料の粉体及び液体
との混合性も良好、肌の乗りも良好である。又、母材と
して無機粉末を球状化させて用いることにより、無機粉
末球表面に形成された無数の細孔のもつ吸着作用によっ
て母材に対するコーテイング量を大幅に増やすことがで
きる。結果、重量割合にして母材40%、コーテイング
材60%を可能とした。これは、コーテイング材の重量
割合がせいぜい20%だった従来と比べ大きな効果であ
る。又、一度コーティングさせたコーティング層の上に
新に別の微粉末でコーティング層を形成させることもコ
ーチイン材の重量割合60%を超えない範囲で可能で、
撥水性のコーテイング材の上に疎水性のコーテイング材
をかぶせて疎水性にしたり、吸油性を増加させることも
可能となる。
Cosmetic materials coated with ultrafine coating powder using an inorganic powder method have excellent properties in the following points. That is, it has good color and gloss, good UV protection effect, good spreadability, good mixability with other cosmetic powders and liquids, and good feel on the skin. Furthermore, by using spheroidized inorganic powder as the base material, the amount of coating on the base material can be significantly increased due to the adsorption effect of the countless pores formed on the surface of the inorganic powder spheres. As a result, the weight ratio of the base material was 40% and the coating material was 60%. This is a large effect compared to the conventional method, in which the weight ratio of the coating material was at most 20%. In addition, it is possible to form a new coating layer using another fine powder on the coating layer that has been coated once, as long as the weight ratio of the coachine material does not exceed 60%.
It is also possible to cover a water-repellent coating material with a hydrophobic coating material to make it hydrophobic or to increase oil absorption.

〔実施例〕〔Example〕

母材の球状粒体にシリカ球を用いコーテイング材として
超微粒子化された酸化チタンの微粉末をシリカ球表面に
コーティングさせた。第1図にその状態を示す。
Silica spheres were used as the spherical particles of the base material, and ultrafine titanium oxide fine powder was coated on the surface of the silica spheres as a coating material. Figure 1 shows the situation.

なお、画素材の配合比は重量換算でシリカ球80%、酸
化チタン20%である。
The composition ratio of the image material is 80% silica spheres and 20% titanium oxide in terms of weight.

a、シリカ球 含水率 2%以下 PH7〜 9 比   重   0.9 平均粒径  2μm 溶融点 1200℃以上 b、酸化チタン 結晶型  ルチル型 表面の性質  親水性 比表面積  約150 rn’/、9 平均粒径  15℃m 乾燥減量  3.0%以下 強熱減量  7.0%以下 次に、この酸化チタンをコーティングしてできたシリカ
球状粒子を使用して(1)パウダーファンデーション、
(2)油性ファンデーションを製造する方法を説明する
。なお、チタンシリカとは酸化チタンの超微粒子をシリ
カ球の表面にコーティングさせた球状粒子で、スーパー
ミクロンマイカ(ホンカワミクロン(彬、商品名)はマ
イカを超微粒子化させたものである。
a, Silica sphere water content 2% or less PH7-9 Specific gravity 0.9 Average particle size 2 μm Melting point 1200°C or moreb, Titanium oxide crystal type Rutile type surface properties Hydrophilic specific surface area Approximately 150 rn'/, 9 Average particle Diameter: 15°Cm Loss on drying: 3.0% or less Loss on ignition: 7.0% or less Next, using the silica spherical particles coated with titanium oxide, (1) powder foundation,
(2) A method for producing an oil-based foundation will be explained. Titanium silica is a spherical particle made by coating the surface of a silica sphere with ultrafine particles of titanium oxide, and Super Micron Mica (Honkawa Micron (trade name)) is an ultrafine particle of mica.

(1)  パウダーファンデーションを製造する場合ま
ず、原料(ト)を混合機(ホンカワミクロン■、商品名
ナウタミキサ)で10分間混合する。次に原料IB)を
乳化機(ホンカワミクロン(掬、商品名デイスパミル)
にて乳化混合し、温度が60℃になれば前記混合機に付
設の噴霧装置により混合機上部より散布し、原料四と共
にそぼろ状になるまで(約15分間)混合する。この時
、混合機内の温度を60℃及至70℃に保つことにより
混合を促進させれる。また、分散の為に混合機下部に取
り付けられた攪拌羽根で攪拌を行わせる事もある。
(1) When producing a powder foundation, first, the raw materials (g) are mixed for 10 minutes in a mixer (Honkawa Micron ■, trade name Nauta Mixer). Next, feed the raw material IB) into an emulsifying machine (Honkawa Micron (trade name: Dispa Mill)).
When the temperature reaches 60° C., it is sprayed from the top of the mixer using a spray device attached to the mixer, and mixed with raw material 4 until it becomes crumbly (about 15 minutes). At this time, mixing can be promoted by maintaining the temperature inside the mixer at 60°C to 70°C. In addition, for dispersion, stirring may be performed using a stirring blade attached to the bottom of the mixer.

また、原料C)に約5%の水を加えて混合し、攪拌しつ
つ乾燥させた後、原料(2)と均一に混合する。
Further, about 5% water is added to raw material C), mixed, dried while stirring, and then mixed uniformly with raw material (2).

これを取り出し粉砕機(ホンカワミクロン(株、商品名
フィッッミル)で解砕させて粒度調整を行い製品とする
This is taken out and crushed in a crusher (Honkawa Micron Co., Ltd., trade name: FIFMIL) to adjust the particle size and produce a product.

(4油性ファンデーションを製造する場合原料(Q  
香   料               0・3%ま
ず、原料(ト)を混合機(たとえば前記ナウタミキサ)
で7分間混合する。
(4 Raw materials for producing oil-based foundation (Q)
Fragrance: 0.3% First, mix the raw materials (g) with a mixer (for example, Nauta mixer).
Mix for 7 minutes.

次に原料(B)を乳化機(たとえば前記ディスパミル)
にて攪拌乳化させ、80℃になれば前記混合機内にスプ
レーし、混合機を90℃まで加熱して約5分程度混合す
る。そして、混合機の温度を50℃まで下げて原料C)
を添加し約5分間混合した後、さらに温度を20℃まで
今加してから取り出し製品とする。
Next, raw material (B) is added to an emulsifying machine (for example, the above-mentioned Dispa Mill).
Stir to emulsify at 80°C, spray into the mixer, heat the mixer to 90°C, and mix for about 5 minutes. Then, lower the temperature of the mixer to 50℃ and raw material C)
After adding and mixing for about 5 minutes, the temperature was further increased to 20°C, and the product was taken out.

以上本発明の実施例として、パウダーファンデーション
と油性ファンデーションの製造方法を記したが、これら
両製品を従来市販品と比較した結果を下表に示す。これ
は、6ケ月間50名の女性に官能評価を依頼した結果で
、評価項目は、のび、つや、肌合感覚、のりの良さ、透
明度、総合評価の以上6項目で行った。なお、Aは本実
施例のチタンシリカ配合品、Bは従来の配合品を示し、
A>BならAの方がBより秀れており、A=Bなら同程
度で余り変らないことを表す。
As examples of the present invention, methods for producing powder foundation and oil-based foundation have been described above, and the results of comparing these two products with conventional commercially available products are shown in the table below. This is the result of asking 50 women to perform sensory evaluations over a 6-month period, and the evaluation items were 6 items: spreadability, gloss, texture, feel, transparency, and overall evaluation. In addition, A indicates the titanium-silica compounded product of this example, B indicates the conventional compounded product,
If A>B, A is better than B, and if A=B, it means that they are of the same level and do not differ much.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、本実施例の化粧料の顕微鏡写真である。 FIG. 1 is a microscopic photograph of the cosmetic of this example.

Claims (3)

【特許請求の範囲】[Claims] (1)無機粉末の一又は複数種を結合し母材とした無機
質球状粒子の表面に超微粒子化させた他の微粉末を一又
は複数種コーティングさせた化粧料。
(1) A cosmetic in which one or more kinds of inorganic powders are bonded together and the surface of inorganic spherical particles used as a base material is coated with one or more kinds of other ultrafine powders.
(2)前記無機粉末は、シリカ、ケイ酸カルシウム、ケ
イ酸アルミニウム、ケイ酸マグネシウム、酸化チタン、
酸化亜鉛、酸化クロム、酸化コバルト、酸化鉄、酸化ジ
ルコニウム、アルミナ、水酸化アルミニウム、水酸化ク
ロム、硫酸バリウム、オキシ塩化ビスマス、タルク、カ
オリン、マンガン、ベントナイト、マイカ、雲母チタン
等を粒径0.1〜30ミクロンに球状化させた特許請求
の範囲第(1)項記載の化粧料。
(2) The inorganic powder may include silica, calcium silicate, aluminum silicate, magnesium silicate, titanium oxide,
Zinc oxide, chromium oxide, cobalt oxide, iron oxide, zirconium oxide, alumina, aluminum hydroxide, chromium hydroxide, barium sulfate, bismuth oxychloride, talc, kaolin, manganese, bentonite, mica, titanium mica, etc., are prepared with a particle size of 0. The cosmetic according to claim (1), which is spheroidized to a size of 1 to 30 microns.
(3)前記コーティング用の微粉末は、シリカ、ケイ酸
カルシウム、ケイ酸アルミニウム、ケイ酸マグネシウム
、酸化チタン、酸化亜鉛、酸化クロム、酸化コバルト、
酸化鉄、酸化ジルコニウム、アルミナ、水酸化アルミニ
ウム、水酸化クロム、硫酸バリウム、オキシ塩化ビスマ
ス、脂肪酸塩、タルク、カオリン、マンガン、ベントナ
イト、マイカ、雲母チタン等の無機粉末、樹脂、油脂等
有機化合物、金、銅、アルミニウム、顔料等を粒径0.
005〜5ミクロンに超微粒子化させてある特許請求の
範囲第(1)項記載の化粧料。
(3) The fine powder for coating includes silica, calcium silicate, aluminum silicate, magnesium silicate, titanium oxide, zinc oxide, chromium oxide, cobalt oxide,
Inorganic powders such as iron oxide, zirconium oxide, alumina, aluminum hydroxide, chromium hydroxide, barium sulfate, bismuth oxychloride, fatty acid salts, talc, kaolin, manganese, bentonite, mica, titanium mica, organic compounds such as resins, oils and fats, Gold, copper, aluminum, pigments, etc. with a particle size of 0.
The cosmetic according to claim (1), which is made into ultrafine particles of 0.005 to 5 microns.
JP24108086A 1986-10-08 1986-10-08 Cosmetic Pending JPS6393707A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24108086A JPS6393707A (en) 1986-10-08 1986-10-08 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24108086A JPS6393707A (en) 1986-10-08 1986-10-08 Cosmetic

Publications (1)

Publication Number Publication Date
JPS6393707A true JPS6393707A (en) 1988-04-25

Family

ID=17068991

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24108086A Pending JPS6393707A (en) 1986-10-08 1986-10-08 Cosmetic

Country Status (1)

Country Link
JP (1) JPS6393707A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0288512A (en) * 1988-09-27 1990-03-28 Shiseido Co Ltd Solid powder cosmetic
JPH02104512A (en) * 1988-10-13 1990-04-17 Agency Of Ind Science & Technol Cosmetic
EP0581651A2 (en) * 1992-07-27 1994-02-02 Suzuki Yushi Industries Co., Ltd. Materials in the form of colored spherical fine particles, processes for producing the same and cosmetic compositions containing the particulate material
EP0679382A1 (en) * 1994-01-27 1995-11-02 Ajinomoto Co., Inc. Silica spheres containing an ultraviolet screen and surface-treated with N-lauroyl-L-lysine powder and cosmetic composition containing them
JPH0840830A (en) * 1994-01-29 1996-02-13 Lucky Co Ltd Pigment for antifungosity make-up goods and its preparation,and make-up composition cotaining said pigment
JP2008260940A (en) * 2000-02-14 2008-10-30 Miyoshi Kasei Inc Novel composite powder and cosmetic containing the same
JP4744040B2 (en) * 2001-09-19 2011-08-10 日揮触媒化成株式会社 Inorganic oxide spherical particles and method for producing the same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS541408A (en) * 1977-06-03 1979-01-08 Mayekawa Mfg Co Ltd Group control method of compressor
JPS5767681A (en) * 1980-10-14 1982-04-24 Ishihara Sangyo Kaisha Ltd Ultraviolet absorber
JPS60169412A (en) * 1984-02-15 1985-09-02 Shiseido Co Ltd Cosmetic

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS541408A (en) * 1977-06-03 1979-01-08 Mayekawa Mfg Co Ltd Group control method of compressor
JPS5767681A (en) * 1980-10-14 1982-04-24 Ishihara Sangyo Kaisha Ltd Ultraviolet absorber
JPS60169412A (en) * 1984-02-15 1985-09-02 Shiseido Co Ltd Cosmetic

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0288512A (en) * 1988-09-27 1990-03-28 Shiseido Co Ltd Solid powder cosmetic
JPH02104512A (en) * 1988-10-13 1990-04-17 Agency Of Ind Science & Technol Cosmetic
JPH0587045B2 (en) * 1988-10-13 1993-12-15 Kogyo Gijutsuin
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