FACIAL MOISTURIZING 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 Technology Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Hydrolyzed Collagen

Inactive ingredient

Aqua, glycerin, titanium dioxide,Tocopherol, DL-Alpha.

Purpose section

Can absorbor reflect ultraviolet rays,Effectively protects skinfrom damage under thesun in outdoor activitycenters.

Warning

Sensitivity testing for newusers. Apply productsparingly to one or twosmall affected areas forthe first 3 days. lf nodiscomfort occurs. Pleasefollow the instructionsabove.

stop use

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

not use

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

OUT OF CHILDREN

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

HOW TO USE

As the final step inyour skin care routine, usebefore makeup. lt ishighly recommended toapply sunscreen at least30 minutes before startingoutdoor activities formaximum effectiveness.

Dosage

It is recommended to use enough sunscreen to cover the entire surface of skin exposed to the sun and reapply every 2 hours after each use, especially after swimming, sweating or wiping the skin.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FACIAL MOISTURIZING SUNSCREEN 
facial moisturizing sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84732-032
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EQUINE COLLAGEN (UNII: 3221SCV0LS) (EQUINE COLLAGEN - UNII:3221SCV0LS)	EQUINE COLLAGEN	1 mg  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
TOCOPHEROL (UNII: R0ZB2556P8)
GLYCERIN (UNII: PDC6A3C0OX)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84732-032-01	50 mL in 1 TUBE; Type 0: Not a Combination Product	10/08/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/08/2024

Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807)

Establishment
Name	Address	ID/FEI	Business Operations
Dongguan Haiyi Technology Co.,Ltd.		722030807	manufacture(84732-032)