ABSOLUT SKIN SPF 50 MOISTURIZING SUNSCREEN- ethylhexyl methoxycinnamate,ethylhexyl salicylate,methylene bis-benzotriazolyl tetramethylbutylphenol,octocrylene cream

Absolut Skin SPF 50 Moisturizing Sunscreen by

Drug Labeling and Warnings

Absolut Skin SPF 50 Moisturizing Sunscreen by is a Otc medication manufactured, distributed, or labeled by Guangzhou Tata Biological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethylhexyl Methoxycinnamate 5%

Ethylhexyl Salicylate 3%

Methylene Bis-benzotriazolyl tetramethylbutyiphenol 2.5%

Octocrylene 2%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Ahigh-performance sunscreen providing broad-spectrum UVA/UVBprotection while hydrating and soothing the skin.

This lightweight,non-greasy formula is infused with advanced UV filters, Vitamin E. andaloe vera to protect against sun damage and nourish the skin.

WARNINGS

For external use only.

DO NOT USE

Avoid contact with eyes; rinse thoroughlyif contact occurs.

STOP USE

Stop use to broken orirritated skin

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun. Limiting sunexposure , wearing protective clothing and using sunscreens mayreduce the risk of skin aging, skin cancer and other harmful effects ofthe sun.

KEEP OUT OF REACH OF CHILDREN

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

INACTIVE INGREDIENT

Water, Glycerin, Butylene Glycol, lsohexadecane, C12-15 AlkylBenzoate, Propylene Glycol Laurate, PhenylTrimethicone,Polysilicone-15,Diethylamino Hydroxybenzoyl Hexyl Benzoate.Hydrogenated Polydecene, Polyglyceryl-3 MethylglucoseDistearate,Potassium Cetyl phosphate, Cetearyl Alcohol.EthylhexylTriazone, Lauric/Myristic/Palmitic/Stearic GlyceridesPentylene Glycol,Tribehenin,Glyceryl Stearate,1.2-Hexanediol.Decyl Glucoside, Propanediol, Acrylates/C10-30 Alkyl AcrylateCrosspolymer, Arginine, Disodium Edta, PentaerythritylTetra-Di-f-Butyl Hydroxyhydrocinnamate, Sodium HyaluronateCaprylhydroxamic Acid, Propylene Glycol, Ethylhexylglycerin,Xanthan Gum

DOSAGE & ADMINISTRATION

Reapplyevery 2 hours when exposed to sunlight.

QUESTIONS

www.myabsolutskin.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ABSOLUT SKIN SPF 50 MOISTURIZING SUNSCREEN 
ethylhexyl methoxycinnamate,ethylhexyl salicylate,methylene bis-benzotriazolyl tetramethylbutylphenol,octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84066-105
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL (UNII: 8NT850T0YS) (METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL - UNII:8NT850T0YS)	METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL	2.5 mg  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2 mg  in 100 mL
ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51) (ETHYLHEXYL METHOXYCINNAMATE - UNII:4Y5P7MUD51)	ETHYLHEXYL METHOXYCINNAMATE	5 mg  in 100 mL
ETHYLHEXYL SALICYLATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	ETHYLHEXYL SALICYLATE	3 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TRIBEHENIN (UNII: 8OC9U7TQZ0)
PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
C14-18 MONO-AND DI-GLYCERIDES (UNII: 82TZ9D9546)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
XANTHAN GUM (UNII: TTV12P4NEE)
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ISOHEXADECANE (UNII: 918X1OUF1E)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
POLYSILICONE-15 (UNII: F8DRP5BB29)
POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE (UNII: W19EIO0DBE)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GLYCERIN (UNII: PDC6A3C0OX)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
PROPYLENE GLYCOL LAURATE (UNII: 668Z5835Z3)
HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)
PROPANEDIOL (UNII: 5965N8W85T)
ARGININE (UNII: 94ZLA3W45F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84066-105-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/10/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	04/10/2025

Labeler - Guangzhou Tata Biological Technology Co., Ltd. (699605102)

Registrant - Guangzhou Tata Biological Technology Co., Ltd. (699605102)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Tata Biological Technology Co., Ltd.		699605102	manufacture(84066-105)