Label: STRONG WHITENING BATH emulsion
- NDC Code(s): 84423-008-01
- Packager: Guangzhou Kadiya Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 26, 2024
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- Official Label (Printer Friendly)
- Purpose section
- Inactive ingredients
- Warning
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USAGE
This Whitening Bath GLUTA TERMINAL WHITE+ is the latest terminal solution designed to solve all types of
skin problems. Lightening of a major nature stretch marks, quintals, black spots, wrinkles, dry skin, acne
pimples and blackheads. Use this whitening bath with its soap and its cream to become very bleash and light. -
DOSAGE
This Whitening Bath GLUTA TERMINAL WHITE+ is the latest terminal solution designed to solve all types of
skin problems. Lightening of a major nature stretch marks, quintals, black spots, wrinkles, dry skin, acne
pimples and blackheads. Use this whitening bath with its soap and its cream to become very bleash and light. - WARNING
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PRINCIPAL DISPLAY PANEL
Active Ingredients
Glutathione0.1%
CARYA ILLINOINENSIS SHELL POWDER0.1%Uses：
For body cleansing, exfoliation and whitening
The storage method：
Store sealed in a cool place and out of sunlightWarning.
1，For external use only, avoid contact with eyes when used
2，Keep out of reach of childrenInactive ingredients：
AQUA，SODIUM LAURETH SULFATE，SODIUM CHLORIDE，COCAMIDOPROPYL BETAINE，GLYCERIN， METHYLISOTHIAZOLINONE，MAGNESIUM NITRATE，MAGNESIUM CHLORIDE
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INGREDIENTS AND APPEARANCE
STRONG WHITENING BATH
strong whitening bath emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84423-008 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE 0.5 mg in 500 mg CARYA ILLINOINENSIS SHELL (UNII: 0QNC8RS9D2) (CARYA ILLINOINENSIS SHELL - UNII:0QNC8RS9D2) CARYA ILLINOINENSIS SHELL 0.5 mg in 500 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) SODIUM LAURETH-2 SULFATE (UNII: ZZQ59TY3KG) GLYCERIN (UNII: PDC6A3C0OX) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) MAGNESIUM NITRATE (UNII: 77CBG3UN78) SODIUM CHLORIDE (UNII: 451W47IQ8X) COCO/OLEAMIDOPROPYL BETAINE (UNII: 5M84PX7JN2) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84423-008-01 500 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/26/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 06/26/2024 Labeler - Guangzhou Kadiya Biotechnology Co., Ltd. (713172913) Establishment Name Address ID/FEI Business Operations Guangzhou Kadiya Biotechnology Co., Ltd. 713172913 manufacture(84423-008)