Label: 7 DAYS ADVANCED WHITENINGSOAP- 7daysadvancedwhiteningsoap soap
- NDC Code(s): 84423-052-01
- Packager: Guangzhou Kadiya Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 3, 2024
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- Official Label (Printer Friendly)
- PURPOSE
- INACTIVE INGREDIENT
- WARNINGS
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PREGNANCY
- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
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PRINCIPAL DISPLAY PANEL
Active Ingredients
Glutathione0.1%
COCOS NUCIFERA(COCONUT)OIL0.1%
Gold0.01%Uses：
For skin cleansing, exfoliation and whitening moisturization
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：
GLYCERIN，WATER，SORBITOL，MALTITOL，MANNITOL，PROPYLENE GLYCOL，WHITE SUGAR，LAURIC ACID，SODIUM LAURETH SULFATE，STEARIC ACID ，SODIUM HYDROXIDE，COCAMIDOPYOPY IBETAINE，ETHYL ALCOHOL，OLEAEUROPAEA(OLIVE)FRUIT OLL，BUTYROSPERMUMPARKII(SHEA)BUTTER，AROMA
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INGREDIENTS AND APPEARANCE
7 DAYS ADVANCED WHITENINGSOAP
7daysadvancedwhiteningsoap soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84423-052 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE 0.25 g in 250 g GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 0.025 g in 250 g COCONUT OIL (UNII: Q9L0O73W7L) (COCONUT OIL - UNII:Q9L0O73W7L) COCONUT OIL 0.25 g in 250 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) MALTITOL (UNII: D65DG142WK) MANNITOL (UNII: 3OWL53L36A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) LAURIC ACID (UNII: 1160N9NU9U) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM HYDROXIDE (UNII: 55X04QC32I) COCO/OLEAMIDOPROPYL BETAINE (UNII: 5M84PX7JN2) SHEA BUTTER (UNII: K49155WL9Y) SORBITOL (UNII: 506T60A25R) SUCROSE (UNII: C151H8M554) STEARIC ACID (UNII: 4ELV7Z65AP) ALCOHOL (UNII: 3K9958V90M) OLIVE OIL (UNII: 6UYK2W1W1E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84423-052-01 250 g in 1 BOX; Type 0: Not a Combination Product 10/03/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 10/03/2024 Labeler - Guangzhou Kadiya Biotechnology Co., Ltd. (713172913) Establishment Name Address ID/FEI Business Operations Guangzhou Kadiya Biotechnology Co., Ltd. 713172913 manufacture(84423-052)