CVS HEALTH  SPF 50 VANISHING ZINC SUN- 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.

----------

CVS Health SPF 50 Vanishing Zinc Sun 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

Other information

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

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, 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.

Label

CVS26037A

CVS26037K

CVS HEALTH   SPF 50 VANISHING ZINC SUN
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-142
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE47 mg  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE49 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
CERAMIDE NG (UNII: C04977SRJ5)  
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)  
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)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-142-0385 g in 1 BOTTLE; Type 0: Not a Combination Product02/03/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35202/03/2017
Labeler - CVS Pharmacy (062312574)

Revised: 11/2022
Document Id: c6a3f429-e970-0b00-e053-2995a90aee88
Set id: 47a21b12-5959-105c-e054-00144ff8d46c
Version: 6
Effective Time: 20221104
 
CVS Pharmacy