CVS HEALTH SPF 50 VANISHING ZINC SUN FACE- titanium dioxide, zinc oxide lotion 
CVS Pharmacy

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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CVS Health SPF 50 Vanishing Zinc Sun Face Lotion

Active ingredients

Titanium Dioxide 4.9%, Zinc Oxide 4.7%

Purpose

Sunscreen

Uses

• helps prevent sunburn • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

​Do not use

​When using this product​

keep out of eyes. Rinse with water to remove.

​Stop use and ask doctor if

​Keep out of reach of children.

​If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

Water, Isohexadecane, Butyloctyl Salicylate, Dimethicone, Cetyl Dimethicone, Styrene/Acrylates Copolymer, VP/Eicosene Copolymer, Trimethylsiloxysilicate, Arachidyl Alcohol, Arachidyl Glucoside, Trisiloxane, Dimethicone PEG-8 Laurate, Butylene Glycol, Polysorbate 60, Hydrated Silica, Ceramide 3, Ceramide 6-II, Ceramide 1, Cholesterol, Niacinamide, Phytosphingosine, PEG-100 Stearate, Glyceryl Stearate, Ascorbic Acid, Avena Sativa (Oat) Kernel Extract, Beeswax, Behenyl Alcohol, Benzyl Alcohol, Stearic Acid, Bisabolol, Dipotassium Glycyrrhizate, Ethylhexylglycerin, Glycerin, Hydroxyethyl Acrylate/sodium Acryloyldimethyl Taurate Copolymer, Pantothenic Acid, PEG-8, Xanthan Gum, Polyaminopropyl Biguanide, Polymethyl Methacrylate, Alumina, Potassium Sorbate, Retinyl Palmitate, Sodium Lauroyl Lactylate, Carbomer, Tocopheryl Acetate, Disodium EDTA, Methicone, Methylisothiazolinone, Castor Oil Phosphate, Triethoxycaprylylsilane.

Other information

• protect the product in this container from excessive heat and direct sun
• may stain or damage some fabrics, materials or surfaces

Label

CVS39008K

CVS HEALTH  SPF 50 VANISHING ZINC SUN FACE
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-143
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE48.3 mg  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE50.6 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
CERAMIDE NP (UNII: 4370DF050B)  
POLIHEXANIDE (UNII: 322U039GMF)  
CERAMIDE 6 II (UNII: F1X8L2B00J)  
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
OAT (UNII: Z6J799EAJK)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
CERAMIDE 1 (UNII: 5THT33P7X7)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
DIMETHICONE PEG-8 LAURATE (UNII: 72MF9C2A18)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)  
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
WATER (UNII: 059QF0KO0R)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PANTOTHENIC ACID (UNII: 19F5HK2737)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CASTOR OIL PHOSPHATE (UNII: SBR4NJI3UJ)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
XANTHAN GUM (UNII: TTV12P4NEE)  
PEG-100 STEARATE (UNII: YD01N1999R)  
DOCOSANOL (UNII: 9G1OE216XY)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
LEVOMENOL (UNII: 24WE03BX2T)  
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
TRISILOXANE (UNII: 9G1ZW13R0G)  
CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)  
METHICONE (20 CST) (UNII: 6777U11MKT)  
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
NIACINAMIDE (UNII: 25X51I8RD4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-143-031 in 1 BOX02/03/2017
1NDC:69842-143-0256 g in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35202/08/2016
Labeler - CVS Pharmacy (062312574)

Revised: 12/2022
Document Id: f04a14db-269c-efc4-e053-2995a90a6323
Set id: 47a504b8-b0d8-030a-e054-00144ff88e88
Version: 6
Effective Time: 20221220
 
CVS Pharmacy