![CVS HEALTH SPF 50 VANISHING ZINC SUN (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [CVS PHARMACY]](https://medic.hrt.org//dailymed/images/47a21b12-5959-105c-e054-00144ff8d46c/RepresentativeImage.jpg)
- Active ingredients
- Purpose
- Uses
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
Directions
- apply liberally 15 minutes before sun exposure
- reapply:
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
- 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 broad spectrum SPF of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeve shirts, pants, hats, and sunglasses
- children under 6 months: ask a doctor
- Other information
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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.
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CVS HEALTH SPF 50 VANISHING ZINC SUN
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-142 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 47 mg in 1 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 49 mg in 1 g Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-142-03 85 g in 1 BOTTLE; Type 0: Not a Combination Product 02/03/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 02/03/2017 Labeler - CVS Pharmacy (062312574) Registrant - Fruit of the Earth, Inc. (079559467) Establishment Name Address ID/FEI Business Operations Fruit Of The Earth Research Laboratories, Inc. 008193513 manufacture(69842-142)
