FACE SUNSCREEN- sunscreen cream

Face Sunscreen by

Drug Labeling and Warnings

Face Sunscreen by is a Otc medication manufactured, distributed, or labeled by Shenzhen Rushen E-commerce Co.. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide 9.0%
Octinoxate 7.5%

PURPOSE

Sunscreen
Moisturizes throughout theday & helps protects

Uses

Apply sunscreen generously to exposedskin. Rub it in evenly. Reapply as neededespecially after swimming or sweating.Enjoy your sun-protected day!

Wamings

For exteral use only

DESCRIPTION

Do not use
on damaged or broken skin

WHEN USING

When using this product
Only for external use. do not ingest.
Avoid direct contact with eyes.

STOP USE

Stop use and ask a doctor if
rash occurs

KEEP OUT OF REACH OF CHILDREN

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

ASK DOCTOR/PHARMACIST

Ask Doctor
When Pregnant or breast-feeding.

DOSAGE & ADMINISTRATION

Directions
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.
-Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging
-To decrease this risk, regularly use a sunscreen with a B road.
-Spectrum SPF value of15 or higher and other sun protection：
-limit time in the sun, especially from 10 a.m.-2 p.m.
-and wear long-sleeved shirts, pants, hats, and sunglasses

STORAGE AND HANDLING

Other information
Before use, read all information on thecarton Store at controlled room temperature20 to 25 C (68 to 77°F)

Inactive ingredients

Water, Glycerin, Cetearyl Alcohol, Butylene Glycol,Niacinamide, Sodium Hyaluronate, Tocopherol, Centella,Asiatica Extract,Camellia Sinensis Leaf Extract,Ethylhexylglycerin, Carbomer, Triethoxycaprylyisilane,Phenoxyethanol,Xanthan Gum,Additional Ingredients(Fragrances,Stabilizers,etc.),Dibutyl Adipate,Polymethylsiisesquioxane,Coco-Caprylate/Caprate,Hyalur

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FACE SUNSCREEN 
sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84431-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 mg  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	9 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
HYDROGENATED POLYISOBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
NIACINAMIDE (UNII: 25X51I8RD4)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84431-001-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	06/01/2024

Labeler - Shenzhen Rushen E-commerce Co.. Ltd. (700135202)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Rushen E-commerce Co.. Ltd.		700135202	manufacture(84431-001)