SUNSCREEN PERFECTION DOUBLE SHIELD cream

SUNSCREEN PERFECTION DOUBLE SHIELD by

Drug Labeling and Warnings

SUNSCREEN PERFECTION DOUBLE SHIELD by is a Otc medication manufactured, distributed, or labeled by Shenzhen XiaoMai Manufacturing Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Niacinamide: 2%
Sodium Hyaluronate: 0.5%
Hyaluronic Acid: 0.1%
Tocopherol: 0.2%
Ethylhexyl Methoxycinnamate: 5%
Octocrylene: 4%
Zinc Oxide: 3%
Centella Asiatica Extract: 1%
Camellia Sinensis Leaf Extract: 1%

PURPOSE

helps prevent sunburn.

Uses

decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS

For external use only.

Do not use

on damaged or broken skin.

When using this product

keep out of eyes.
Rinse with water to remove.

Stop use and ask a doctor

if rash occurs.

Keep out of reach of children.

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

Directions for use

apply liberally 15 minutes before sun exposure.
reapply at least every 2 hours.
use a water resistant sunscreen if swimming or sweating.

INACTIVE INGREDIENT

Aqua: 65%
Glycerin: 3%
Cetearyl Alcohol: 2%
Butylene Glycol: 3%
Ethylhexylglycerin: 0.1%
Xanthan Gum: 0.2%
Phenoxyethanol: 0.8%
Carbomer: 0.2%
OTV: 5%
Triethoxycaprylylsilane: 0.1%
Dibutyl Adipate: 2%
Polymethylsilsesquioxane: 1.7%
Linalool: 0.1%

Other Information

Protect the product in this container from excessive heat and direct sun.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUNSCREEN PERFECTION DOUBLE SHIELD 
sunscreen perfection double shield cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83872-050
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	2 mg  in 1 g
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	20 mg  in 1 g
HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONIC ACID	1 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	30 mg  in 1 g
GLYCERIN (UNII: PDC6A3C0OX)	30 mg  in 1 g
WATER (UNII: 059QF0KO0R)	650 mg  in 1 g

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83872-050-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	03/17/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	03/17/2024

Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen XiaoMai Manufacturing Co., Ltd.		712999147	manufacture(83872-050)