Label: DRUGGIST KOJIC ACID DARK SPOT REMOVER capsule
- NDC Code(s): 83872-140-01
- Packager: Shenzhen XiaoMai Manufacturing Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 12, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- Uses
- WARNINGS
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
- Directions for use
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INACTIVE INGREDIENT
Stearic Acid: 15%
Lauric Acid: 9%
Glycerin: 18%
Sodium Hydroxide: 0.5%
Sodium Laureth Sulfate: 6%
Disodium EDTA: 0.7%
Sucrose Laurate: 2%
BHT: 0.6%
Propylene Glycol Dioleate: 3.1%
Decyl Glucoside: 7%
Shea Butter Oleyl Esters: 4%
PPG-25 Sorbitol: 2%
Olive Oil: 3%
PEG-10 Esters: 2%
HC Yellow No.5: 0.1%
Ascorbic Acid : 3%
Tocopherol : 3% - Other Information
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DRUGGIST KOJIC ACID DARK SPOT REMOVER
druggist kojic acid dark spot remover capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83872-140 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONIC ACID 30 mg in 1 g RETINOL (UNII: G2SH0XKK91) (RETINOL - UNII:G2SH0XKK91) RETINOL 30 mg in 1 g KOJIC ACID (UNII: 6K23F1TT52) (KOJIC ACID - UNII:6K23F1TT52) KOJIC ACID 70 mg in 1 g Inactive Ingredients Ingredient Name Strength SODIUM LAURETH SULFATE (UNII: BPV390UAP0) 60 mg in 1 g GLYCERIN (UNII: PDC6A3C0OX) 180 mg in 1 g PROPYLENE GLYCOL DIOLEATE (UNII: 84T0LSN7U6) 31 mg in 1 g OLIVE OIL (UNII: 6UYK2W1W1E) 30 mg in 1 g SUCROSE LAURATE (UNII: 05Q7CD0E49) 20 mg in 1 g SODIUM HYDROXIDE (UNII: 55X04QC32I) 5 mg in 1 g HC YELLOW NO. 5 (UNII: I844A312T7) 1 mg in 1 g STEARIC ACID (UNII: 4ELV7Z65AP) 150 mg in 1 g LAURIC ACID (UNII: 1160N9NU9U) 90 mg in 1 g BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) 6 mg in 1 g DECYL GLUCOSIDE (UNII: Z17H97EA6Y) 70 mg in 1 g ASCORBIC ACID (UNII: PQ6CK8PD0R) 30 mg in 1 g TOCOPHEROL (UNII: R0ZB2556P8) 30 mg in 1 g Product Characteristics Color orange Score no score Shape RECTANGLE Size 75mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83872-140-01 135 g in 1 BOTTLE; Type 0: Not a Combination Product 05/13/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 05/13/2024 Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147) Establishment Name Address ID/FEI Business Operations Shenzhen XiaoMai Manufacturing Co., Ltd. 712999147 manufacture(83872-140)