BRIGHTENING GEL CREAM- ojw brightening gel cream emulsion

Brightening Gel Cream by

Drug Labeling and Warnings

Brightening Gel Cream by is a Otc medication manufactured, distributed, or labeled by Guangzhou Meiya Cosmetics Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

IACINAMIDE 2%

PURPOSE

Function: Crystal gel texture, clear and easy to absorb, contains camellia extract plant essence ingredients, moisturizes the skin, invigorates and softens the skin resistance, leaving the skin delicate and elastic.

INDICATIONS & USAGE

HOW TO USE : After washing your face, take an appropriate amount of gel about 1-2cm, gently massage your face with your fingers and abdomen from inside to outside, and rinse with water.

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.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.

3. 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.

WHEN USING

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.

KEEP OUT OF REACH OF CHILDREN

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.

DOSAGE & ADMINISTRATION

After washing your face, take an appropriate amount of gel about 1-2cm, gently massage your face with your fingers and abdomen from inside to outside, and rinse with water.

INACTIVE INGREDIENT

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BRIGHTENING GEL CREAM 
ojw brightening gel cream emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84673-004
Route of Administration	AURICULAR (OTIC), CONJUNCTIVAL, BUCCAL, DENTAL, CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 1 mg

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)	1 g  in 1 mg
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	1.1 g  in 1 mg
TREHALOSE (UNII: B8WCK70T7I)	1.1 g  in 1 mg
LAURETH-7 (UNII: Z95S6G8201)	0.035 g  in 1 mg
BETAINE (UNII: 3SCV180C9W)	1.1 g  in 1 mg
FOLIC ACID (UNII: 935E97BOY8)	1 g  in 1 mg
HEXYLENE GLYCOL (UNII: KEH0A3F75J)	1 g  in 1 mg
1,2-HEXANEDIOL (UNII: TR046Y3K1G)	0.00048 g  in 1 mg
METHYLPARABEN (UNII: A2I8C7HI9T)	0.15 g  in 1 mg
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.45 g  in 1 mg
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	1 g  in 1 mg
GLYCERIN (UNII: PDC6A3C0OX)	5 g  in 1 mg
HYDROXYPROPYL TETRAHYDROPYRANTRIOL (UNII: 4U3GMG1OT1)	1 g  in 1 mg
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)	0.175 g  in 1 mg
WATER (UNII: 059QF0KO0R)	88.5 g  in 1 mg
ETHYLHEXYL PALMITATE (UNII: 2865993309)	1 g  in 1 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84673-004-04	50 mg in 1 BOTTLE; Type 0: Not a Combination Product	04/15/2024	04/15/2027

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/15/2024	04/15/2027

Labeler - Guangzhou Meiya Cosmetics Co.,Ltd. (553030421)