Label: GLUTATHIONESKINWHITENINGLOTION- glutathione skin whitening lotion emulsion
- NDC Code(s): 84423-061-01
- Packager: 713172913
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
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- Official Label (Printer Friendly)
- PURPOSE
- INACTIVE INGREDIENT
- WARNINGS
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- KEEP OUT OF REACH OF CHILDREN
- ACTIVE INGREDIENT
-
PRINCIPAL DISPLAY PANEL
Active Ingredients Purpose
Glutathione0.5% Whitening
ASCORBIC ACID1% Whitening
DAUCUS CAROTA FRUIT OIL2% Moisturizing
NIACINAMIDE5% Whitening
SODIUM HYALURONATE1% Moisturizing
Uses:
For body moisturisation 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、CETEARYL ALCOHOL、PARAFFINUM LIQUIDUM、DIMETHICONE、GLYCERIN、POLYACRYLAMIDE、CETEARETH-25、LAURIC/MYRISTIC/PALMITIC/STEARIC、GLYCERIDES、DMDM HYDANTOIN、METHYLPARABEN、PROPYLPARABEN、XANTHAN GUM、SODIUM HYDROXIDE、 METHYLISOTHIAZOLINONE,ALLANTOIN -
INGREDIENTS AND APPEARANCE
GLUTATHIONESKINWHITENINGLOTION
glutathione skin whitening lotion emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84423-061 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DAUCUS CAROTA SATIVA (CARROT) SEED OIL (UNII: 595AO13F11) (DAUCUS CAROTA SATIVA (CARROT) SEED OIL - UNII:595AO13F11) DAUCUS CAROTA SATIVA (CARROT) SEED OIL 4 g in 400 mL GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE 2 g in 400 mL ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 2 g in 400 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 20 g in 400 mL Inactive Ingredients Ingredient Name Strength PARAFFINUM LIQUIDUM (UNII: T5L8T28FGP) DMDM HYDANTOIN (UNII: BYR0546TOW) AQUA (UNII: 059QF0KO0R) CETEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE 1000 (UNII: MCU2324216) PROPYLPARABEN (UNII: Z8IX2SC1OH) SODIUM HYDROXIDE (UNII: 55X04QC32I) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) GLYCERIN (UNII: PDC6A3C0OX) POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I) ALLANTOIN (UNII: 344S277G0Z) CETEARETH-25 (UNII: 8FA93U5T67) METHYLPARABEN (UNII: A2I8C7HI9T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84423-061-01 400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/18/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 12/18/2024 Labeler - 713172913 (713172913) Establishment Name Address ID/FEI Business Operations Guangzhou Kadiya Biotechnology Co., Ltd. 713172913 manufacture(84423-061)