Label: KNUCKLE PEELINGSOAP- knucklepeelingsoap soap
- NDC Code(s): 84423-049-01
- Packager: Guangzhou Kadiya Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 28, 2024
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- Official Label (Printer Friendly)
- PURPOSE
- INACTIVE INGREDIENT
- WARNINGS
- DOSAGE & ADMINISTRATION
- KEEP OUT OF REACH OF CHILDREN
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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PRINCIPAL DISPLAY PANEL
Active Ingredients
GLUTATHIONE0.49%
Alpha Arbutin0.1%
ASCORBIC ACID0.5%
Gold0.01%
Uses：
For cleansing, exfoliating, Lightening and moisturising the skin.
Indications: For skin whitening cleansing exfoliation
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：
GLYCERIN、WATER、SORBITOL、MALTITOL、MANNITOL、PROPYLENE、GLYCOL、WHITE SUGAR、LAURIC ACID、SODIUM LAURETH SULFATE、COCOS、NUCIFERA(COCONUT)OIL、STEARIC ACID 、SODIUM HYDROXIDE、COCAMIDOPYOPY、IBETAINE、ETHYL ALCOHOL、AROMA
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INGREDIENTS AND APPEARANCE
KNUCKLE PEELINGSOAP
knucklepeelingsoap soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84423-049 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 1.25 g in 250 g GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE 1.225 g in 250 g GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 0.025 g in 250 g ALPHA-ARBUTIN (UNII: 72VUP07IT5) (ALPHA-ARBUTIN - UNII:72VUP07IT5) ALPHA-ARBUTIN 0.25 g in 250 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) SUCROSE (UNII: C151H8M554) STEARIC ACID (UNII: 4ELV7Z65AP) MALTITOL (UNII: D65DG142WK) MANNITOL (UNII: 3OWL53L36A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) COCONUT OIL (UNII: Q9L0O73W7L) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITOL (UNII: 506T60A25R) LAURIC ACID (UNII: 1160N9NU9U) COCO/OLEAMIDOPROPYL BETAINE (UNII: 5M84PX7JN2) WATER (UNII: 059QF0KO0R) SHEA BUTTER (UNII: K49155WL9Y) ALCOHOL (UNII: 3K9958V90M) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84423-049-01 250 g in 1 CARTON; Type 0: Not a Combination Product 09/29/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 09/29/2024 Labeler - Guangzhou Kadiya Biotechnology Co., Ltd. (713172913) Establishment Name Address ID/FEI Business Operations Guangzhou Kadiya Biotechnology Co., Ltd. 713172913 manufacture(84423-049)