Label: EXTREME SHINE BODYLOTION emulsion
- NDC Code(s): 84423-026-01
- Packager: Guangzhou Kadiya Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 23, 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、METHYLPARABEN、CARBOMER、ALLANTOIN、TRIETHANOLAMINE、AROMA、SODIUM METABISULFITE、PROPYLPARABEN、DISODIUM EDTA、3-o-ETHYL ASCORBIC ACID
- WARNINGS
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- ACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
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PRINCIPAL DISPLAY PANEL
Drug Facts
Active Ingredients
PYRUS MALUS FRUIT EXTRACT 0.5%
KOJIC DIPALMITATE 0.39%
NIACINAMIDE 1.04%
Uses：
For Brightening Skin Tone
The storage method：
Store sealed in a cool place and out of sunlight
Warning.
1.Before use, perform a skin test on your arm and discontinue use if you have allergy symptoms or skin abnormalities.
2、For external use only, avoid contact with eyes when used
3、Keep out of reach of children
Inactive 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、METHYLPARABEN、CARBOMER、ALLANTOIN、TRIETHANOLAMINE、AROMA、SODIUM METABISULFITE、PROPYLPARABEN、DISODIUM EDTA、3-o-ETHYL ASCORBIC ACID
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INGREDIENTS AND APPEARANCE
EXTREME SHINE BODYLOTION
extreme shine bodylotion emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84423-026 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 5.2 mg in 500 mL APPLE (UNII: B423VGH5S9) (APPLE - UNII:B423VGH5S9) APPLE 2.5 mg in 500 mL KOJIC DIPALMITATE (UNII: 13N249RWTM) (KOJIC DIPALMITATE - UNII:13N249RWTM) KOJIC DIPALMITATE 1.95 mg in 500 mL Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) DMDM HYDANTOIN (UNII: BYR0546TOW) C13-16 ISOPARAFFIN (UNII: LED42LZG6O) MINERAL OIL (UNII: T5L8T28FGP) TROLAMINE (UNII: 9O3K93S3TK) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) ALLANTOIN (UNII: 344S277G0Z) UREA (UNII: 8W8T17847W) PEG-100 STEARATE (UNII: YD01N1999R) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) SODIUM METABISULFITE (UNII: 4VON5FNS3C) PROPYLPARABEN (UNII: Z8IX2SC1OH) 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) METHYLPARABEN (UNII: A2I8C7HI9T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84423-026-01 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/24/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 07/24/2024 Labeler - Guangzhou Kadiya Biotechnology Co., Ltd. (713172913) Establishment Name Address ID/FEI Business Operations Guangzhou Kadiya Biotechnology Co., Ltd. 713172913 manufacture(84423-026)