Label: ULTIMATE WHITENING BODYLOTION- ultimatewhiteningbodylotion emulsion
- NDC Code(s): 84423-047-01
- Packager: Guangzhou Kadiya Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PURPOSE
-
INACTIVE INGREDIENT
AQUA，MINERAL OIL，GLYCERIN，CETEARYL ALCOHOL，UREA，GLYCERYL STEARATE，PEG-100 STEARATE，CETEARETH-20，POTASSIUM CETYL PHOSPHATE，C13-16 ISOPARAFFIN，DIMETHICONE，DMDM HYDANTOIN，BUTYLENE GLYCOL，IODOPROPYNYL BUTYLCARBAMATE，AROMA，METHYLPARABEN，CARBOMER，ALLANTOIN，TRIETHANOLAMINE，PROPYLPARABEN，DISODIUM EDTA，3-o-ETHYL ASCORBIC ACID
- WARNINGS
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- KEEP OUT OF REACH OF CHILDREN
- ACTIVE INGREDIENT
-
PRINCIPAL DISPLAY PANEL
Active Ingredients
Glutathione1.5%
KOJIC ACID1%
NIACINAMIDE2%
Uses：
For Body Skin Whitening and Moisturising
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，MINERAL OIL，GLYCERIN，CETEARYL ALCOHOL，UREA，GLYCERYL STEARATE，PEG-100 STEARATE，CETEARETH-20，POTASSIUM CETYL PHOSPHATE，C13-16 ISOPARAFFIN，DIMETHICONE，DMDM HYDANTOIN，BUTYLENE GLYCOL，IODOPROPYNYL BUTYLCARBAMATE，AROMA，METHYLPARABEN，CARBOMER，ALLANTOIN，TRIETHANOLAMINE，PROPYLPARABEN，DISODIUM EDTA，3-o-ETHYL ASCORBIC ACID
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INGREDIENTS AND APPEARANCE
ULTIMATE WHITENING BODYLOTION
ultimatewhiteningbodylotion emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84423-047 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 10 g in 500 mL KOJIC ACID (UNII: 6K23F1TT52) (KOJIC ACID - UNII:6K23F1TT52) KOJIC ACID 5 g in 500 mL GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE 7.5 g in 500 mL Inactive Ingredients Ingredient Name Strength CARBOMER (UNII: 0A5MM307FC) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERYL STEARATE (UNII: 230OU9XXE4) CETEARYL ALCOHOL (UNII: 2DMT128M1S) DMDM HYDANTOIN (UNII: BYR0546TOW) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) PEG-100 STEARATE (UNII: YD01N1999R) CETEARETH-20 (UNII: YRC528SWUY) METHYLPARABEN (UNII: A2I8C7HI9T) GLYCERIN (UNII: PDC6A3C0OX) AQUA (UNII: 059QF0KO0R) MINERAL OIL (UNII: T5L8T28FGP) ALLANTOIN (UNII: 344S277G0Z) PROPYLPARABEN (UNII: Z8IX2SC1OH) 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) C13-16 ISOPARAFFIN (UNII: LED42LZG6O) DIMETHICONE 1000 (UNII: MCU2324216) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) TRIETHANOLAMINE (UNII: 9O3K93S3TK) UREA (UNII: 8W8T17847W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84423-047-01 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/17/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 12/17/2024 Labeler - Guangzhou Kadiya Biotechnology Co., Ltd. (713172913) Establishment Name Address ID/FEI Business Operations Guangzhou Kadiya Biotechnology Co., Ltd. 713172913 manufacture(84423-047)