WHITENING- ojw brightening serum emulsion

whitening by

Drug Labeling and Warnings

whitening 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

NIACINAMIDE 2%
3-o-ETHYL ASCORBIC ACID 0.15%

PURPOSE

Function:Contains niacinamide and sodium hyaluronate essence, penetrates the skin, moisturizes the skin, nourishes the base of the skin, closes pores, and moisturizes the skin at the same time, softens the skin, refreshes the skin.

INDICATIONS & USAGE

HOW TO USE :After cleansing the skin in the morning and evening,

apply an appropriate amount of essence evenly to the face and massage it to absorb.

WARNINGS

Precautions:

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.
6.Store in a dry place at room temperature.

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. 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.

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.

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.
6.Store in a dry place at room temperature.

DOSAGE & ADMINISTRATION

After cleansing the skin in the morning and evening,

apply an appropriate amount of essence evenly to the face and massage it to absorb.

INACTIVE INGREDIENT

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WHITENING 
ojw brightening serum emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84673-003
Route of Administration	CONJUNCTIVAL, CUTANEOUS, BUCCAL, AURICULAR (OTIC)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 1 mg
3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) (3-O-ETHYL ASCORBIC ACID - UNII:6MW60CB71P)	3-O-ETHYL ASCORBIC ACID	0.15 g  in 1 mg

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	0.01 g  in 1 mg
GLYCERIN (UNII: PDC6A3C0OX)	5 g  in 1 mg
WATER (UNII: 059QF0KO0R)	84.9 g  in 1 mg
METHYLPARABEN (UNII: A2I8C7HI9T)	0.35 g  in 1 mg
1,2-HEXANEDIOL (UNII: TR046Y3K1G)	1 g  in 1 mg
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.5 g  in 1 mg
PEG/PPG-14/7 DIMETHYL ETHER (UNII: 6DNW9T7YT2)	1 g  in 1 mg
TREHALOSE (UNII: B8WCK70T7I)	2 g  in 1 mg
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S AT 0.5%) (UNII: YY2HMJ9NZF)	0.25 g  in 1 mg
XANTHAN GUM (UNII: TTV12P4NEE)	0.1 g  in 1 mg
HYDROXYPROPYL TETRAHYDROPYRANTRIOL (UNII: 4U3GMG1OT1)	0.1 g  in 1 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84673-003-03	100 mg in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2024	04/16/2027

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/16/2024	04/16/2027

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