GZE MULTI-EFFECT WHITENING SUNSCREEN- titanium dioxide,zinc oxide cream

GZE Multi-Effect Whitening Sunscreen by

Drug Labeling and Warnings

GZE Multi-Effect Whitening Sunscreen 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 ingredients

Cannabis Sativa Leaf Extract 15.36%

Ascorbic Acid 10%

Titanium Dioxide 10%

Zinc Oxide 10%

Niacinamide 2%

Purpose

For sunscreen use.

Uses

Apply liberally 15 minutes before sun exposure.

WARNINGS

For external use only.

Stop use and ask a doctor if

rash occurs.

Do not use

Do not use on damaged or broken.

When using this product

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Squeeze out an appropriate amount of sunscreen and spread evenly on skin.

INACTIVE INGREDIENT

NIACINAMIDE
GLYCERIN
WATER O-15
PEG-9 DIGLYCIDYL ETHERISODIUM HYALURONATE CROSSPOLYMER
TREHALOSE
ALLANTOIN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GZE MULTI-EFFECT WHITENING SUNSCREEN 
titanium dioxide,zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83566-122
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	10 mg  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	10 mg  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	10 mg  in 1 g
CANNABIS SATIVA LEAF (UNII: A718Z7DA1K) (CANNABIS SATIVA LEAF - UNII:A718Z7DA1K)	CANNABIS SATIVA LEAF	15.36 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
NIACINAMIDE (UNII: 25X51I8RD4)
GLYCERIN (UNII: PDC6A3C0OX)
WATER O-15 (UNII: 63M8RYN44N)
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)
TREHALOSE (UNII: B8WCK70T7I)
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83566-122-01	60 g in 1 BOTTLE; Type 0: Not a Combination Product	12/20/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/20/2023

Labeler - Guangzhou Yilong Cosmetics Co.,Ltd. (712647107)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Yilong Cosmetics Co.,Ltd.		712647107	manufacture(83566-122)