EVERYRAY SUNCARE SUNSHINE SERUM liquid

EVERYRAY SUNCARE SUNSHINE SERUM by

Drug Labeling and Warnings

EVERYRAY SUNCARE SUNSHINE SERUM by is a Otc medication manufactured, distributed, or labeled by Guangzhou Fantesy Biotechnology Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Zinc Oxide 25%

Purpose

Sunscreen

Uses

Helps prevent sunburn

Warnings

Skin Cancer / skin Aging Alert: Spending time in the sun increasesyour risk of skin cancer and early skiraging . This product has been shownonly to help prevent sunburn , not skincancer or early skin aging.

For external use only .

Do not use

Do not use on damaged or broken skin.

When using this product

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

Stop use

Stop use and ask a doctor if rash occurs.

Keep out of

Keep out of reach of children . If product is swallowed . get medical help or contact a Poison Control Center right away.

Directions

Apply liberally and evenly 15 minutesbefore sun exposure.

Reapply at least every 2 hours.

Use a water resistant sunscreen if swimming or sweating.

Children under 6 months : Ask a doctor.

Other information

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

Inactive ingredients

Water , Squalane , Shea Butter EthyEsters , Isoamyl Laurate , Polygly ceryl-3Ricindleate , Buty octyl SalicylatePropanediol , Isopropyl Isostearate ,Polyglyceryl-3 Diisostearate, Methyipropanediol , Niacinamide , SodiumChloride , Lecithin Caprylyl GlycolPanthenol ( itamin B5 ) , Vitamin C , SilicaAloe Barbadensis Leaf Juice PowderBisabolol, Hvdrolvzed SodiumHyaluronate , Allantoin , PhenylpropanolSodium Myristoyl Glutamate , SodiumHyaluronate , Tetrasodium GlutamateDiacetate , Aluminum HydroxidePolyhydroxysteanic Acid

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EVERYRAY SUNCARE SUNSHINE SERUM 
everyray suncare sunshine serum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83447-002
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	12 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
WATER (UNII: 059QF0KO0R)
SQUALANE (UNII: GW89575KF9)
SHEA BUTTER ETHYL ESTERS (UNII: V2CI786FPG)
SODIUM MYRISTOYL GLUTAMATE (UNII: AYU7QD893W)
ISOAMYL LAURATE (UNII: M1SLX00M3M)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENYLPROPANOL (UNII: 0F897O3O4M)
HYALURONIC ACID (UNII: S270N0TRQY)
POLYHYDROXYSTEARIC ACID STEARATE (UNII: 8KQ7I65XZE)
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
PROPANEDIOL (UNII: 5965N8W85T)
NIACINAMIDE (UNII: 25X51I8RD4)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
LEVOMENOL (UNII: 24WE03BX2T)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
PANTHENOL (UNII: WV9CM0O67Z)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
ALLANTOIN (UNII: 344S277G0Z)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83447-002-01	50 mL in 1 BOX; Type 0: Not a Combination Product	09/25/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	09/25/2023

Labeler - Guangzhou Fantesy Biotechnology Co.,Ltd (619047084)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Fantesy Biotechnology Co.,Ltd		619047084	manufacture(83447-002)