FACIAL MOISTURIZING SUNSCREEN- sunscreen cream

Facial moisturizing sunscreen by

Drug Labeling and Warnings

Facial moisturizing sunscreen by is a Otc medication manufactured, distributed, or labeled by Dongguan Haiyi Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Titanium Dioxide

INACTIVE INGREDIENT

Aqua，Glycerin，Hydrolyzed Collagen，Tocopherol，DL-Alpha

PURPOSE

Apply an adequate amount (about a coin-sized portion or 2mg/cm²) evenly to the face and neck.

WARNINGS

Sensitivity testing for new users. Apply product sparingly to one or twosmall affected areas forthe first 3 days. lf no discomfort occurs. Please follow the instructions above.

STOP USE

his product may cause allergic reactions in asmall number of people.
lf you experience any discomfort,please stop using it immediately.

DO NOT USE

Not suitable for use by children, pregnantor breast feeding people.

KEEP OUT OF REACH OF CHILDREN

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

INDICATIONS & USAGE

As the final step inyour skin care routine, use before makeup. lt is highly recommended to apply sunscreen at least30 minutes before starting outdoor activities for maximum effectiveness.

DOSAGE & ADMINISTRATION

Apply an adequate amount (about a coin-sized portion or 2mg/cm²) evenly to the face and neck.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FACIAL MOISTURIZING SUNSCREEN 
sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85594-004
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROLYZED PORCINE COLLAGEN (ENZYMATIC; 3000 MW) (UNII: 0K9R94573C)
TOCOPHEROL (UNII: R0ZB2556P8)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
AQUA (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85594-004-01	50 mL in 1 TUBE; Type 0: Not a Combination Product	05/12/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/12/2025

Labeler - Dongguan Haiyi Cosmetics Co., Ltd. (570250975)

Registrant - Dongguan Haiyi Cosmetics Co., Ltd. (570250975)

Establishment
Name	Address	ID/FEI	Business Operations
Dongguan Haiyi Cosmetics Co., Ltd.		570250975	manufacture(85594-004)