GZE BRIGHTENNG EXFOLIATING GEL- allantoin 0.5% niacinamide 5% gel

GZE Brightenng Exfoliating Gel by

Drug Labeling and Warnings

GZE Brightenng Exfoliating Gel by is a Otc medication manufactured, distributed, or labeled by Guangzhou Yilong Cosmetics Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Allantoin

Niacinamide

INACTIVE INGREDIENT

Aqua

Butylene Glycol

Glycerin

Carbomer

Trehalose

Hydrolyzed Collagen

Aloe Barbadensis Leaf Extract

Hamamelis Virginiana (Witch Hazel) Extract

Centella Asiatica Extract

Phenoxyethanol

Ethylhexylglycerin

PEG-40 Hydrogenated Castor Oil

Fragrance

INDICATIONS & USAGE

After cleansing face, take appropriateproducts
smear on the face. Along the skin texture and gently massagein circular
motions for 1-2 minutes, until thedead skin off the dirt.The rinse with water.

PURPOSE

Exfoliating.

WARNINGS

For external use only.

STOP USE

Stop use and ask a doctor if rash occurs.

DO NOT USE

Do not use on damaged or broken skin.

WHEN USING

When using this product keep out of eyes. Rinse with water to remove.

KEEP OUT OF REACH OF CHILDREN

1. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

After cleansing face, take appropriateproducts
smear on the face. Along the skin texture and gently massagein circular
motions for 1-2 minutes, until thedead skin off the dirt.The rinse with water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GZE BRIGHTENNG EXFOLIATING GEL 
allantoin 0.5% niacinamide 5% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74458-037
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 g  in 100 g
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
HUMAN TYPE I COLLAGEN (UNII: PT3TGI7OIP)
ALOE BARBADENSIS LEAF EXTRACT (UNII: ZY81Z83H0X)
HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF EXTRACT (UNII: T07U1161SV)
GLYCERIN (UNII: PDC6A3C0OX)
TREHALOSE (UNII: B8WCK70T7I)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PEG-40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
AQUA (UNII: 059QF0KO0R)
CARBOMER (UNII: 0A5MM307FC)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74458-037-01	50 g in 1 TUBE; Type 0: Not a Combination Product	11/03/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/03/2024

Labeler - Guangzhou Yilong Cosmetics Co., Ltd (420929116)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Yilong Cosmetics Co., Ltd		420929116	manufacture(74458-037)