Label: NIACINAMIDE BRIGHTENING FACIAL CLEANSER- ojw niacinamide brightening facial cleanser emulsion
- NDC Code(s): 84673-006-06
- Packager: Guangzhou Meiya Cosmetics Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 17, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
1. This product is for external use only and is not edible;
2. Avoid eye contact, if accidentally into the eyes, please rinse with water immediately;
3. Do not use it if you have dermatitis or skin damage;
4. Depending on the individual's physical condition, before use,It is recommended to have an allergy test behind the ear and stop using it immediately if you feel unwell.
5. Please keep it out of reach of children, Beware of Children's Mis-eating, and children under the age of 3 should not use it.
-
STOP USE
1. Avoid eye contact, if accidentally into the eyes, please rinse with water immediately;
2. Do not use it if you have dermatitis or skin damage;
3. Depending on the individual's physical condition, before use,It is recommended to have an allergy test behind the ear and stop using it immediately if you feel unwell.
-
DO NOT USE
1. This product is for external use only and is not edible;
2. Avoid eye contact, if accidentally into the eyes, please rinse with water immediately;
3. Do not use it if you have dermatitis or skin damage;
4. Depending on the individual's physical condition, before use,It is recommended to have an allergy test behind the ear and stop using it immediately if you feel unwell.
- KEEP OUT OF REACH OF CHILDREN
- WHEN USING
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
NIACINAMIDE BRIGHTENING FACIAL CLEANSER
ojw niacinamide brightening facial cleanser emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84673-006 Route of Administration CONJUNCTIVAL, BUCCAL, DENTAL, CUTANEOUS, AURICULAR (OTIC) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 1 g in 1 mg RESVERATROL (UNII: Q369O8926L) (RESVERATROL - UNII:Q369O8926L) RESVERATROL 1 g in 1 mg Inactive Ingredients Ingredient Name Strength LAURIC ACID (UNII: 1160N9NU9U) 4 g in 1 mg ALANINE (UNII: OF5P57N2ZX) 1 g in 1 mg GLUTAMIC ACID (UNII: 3KX376GY7L) 1 g in 1 mg VALINE (UNII: HG18B9YRS7) 1 g in 1 mg HYDROXYPROPYL TETRAHYDROPYRANTRIOL (UNII: 4U3GMG1OT1) 1 g in 1 mg SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) 1 g in 1 mg POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) 1 g in 1 mg GLYCINE (UNII: TE7660XO1C) 1 g in 1 mg HEXAPEPTIDE-9 (UNII: L25414IE41) 1 g in 1 mg SERINE (UNII: 452VLY9402) 1 g in 1 mg ASPARTIC ACID (UNII: 30KYC7MIAI) 1 g in 1 mg 1,2-HEXANEDIOL (UNII: TR046Y3K1G) 1 g in 1 mg PHENOXYETHANOL (UNII: HIE492ZZ3T) 1 g in 1 mg SODIUM BENZOATE (UNII: OJ245FE5EU) 0.17 g in 1 mg METHYLPARABEN (UNII: A2I8C7HI9T) 0.2 g in 1 mg STEARIC ACID (UNII: 4ELV7Z65AP) 1 g in 1 mg PALMITIC ACID (UNII: 2V16EO95H1) 1.38 g in 1 mg PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) 0.5 g in 1 mg FOLIC ACID (UNII: 935E97BOY8) 1 g in 1 mg SODIUM LACTATE (UNII: TU7HW0W0QT) 1 g in 1 mg HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) 1 g in 1 mg ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) 1 g in 1 mg ACETYL TETRAPEPTIDE-5 (UNII: Y1DFQ308G8) 1 g in 1 mg CETEARETH-25 (UNII: 8FA93U5T67) 1 g in 1 mg PROLINE (UNII: 9DLQ4CIU6V) 1 g in 1 mg CARNOSINE (UNII: 8HO6PVN24W) 1 g in 1 mg LAURETH-7 (UNII: Z95S6G8201) 0.07 g in 1 mg PROPYLPARABEN (UNII: Z8IX2SC1OH) 0.1 g in 1 mg WATER (UNII: 059QF0KO0R) 46.769 g in 1 mg LEUCINE (UNII: GMW67QNF9C) 1 g in 1 mg GLYCERIN (UNII: PDC6A3C0OX) 0.1 g in 1 mg ISOLEUCINE (UNII: 04Y7590D77) 1 g in 1 mg ARGININE (UNII: 94ZLA3W45F) 1 g in 1 mg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84673-006-06 100 mg in 1 BOTTLE; Type 0: Not a Combination Product 04/14/2024 04/14/2027 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 04/14/2024 04/14/2027 Labeler - Guangzhou Meiya Cosmetics Co., Ltd. (553030421)