Label: CVS HEALTH SPF 30 ULTRA SHEER- avobenzone, homosalate, octinoxate, octisalate, oxybenzone lotion
- NDC Code(s): 69842-118-09
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated November 11, 2022
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Keep out of reach of children.
- Stop use and ask a doctor
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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 value 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-sleeved shirts, pants, hats, and sunglasses
• children under 6 months: Ask a doctor -
Inactive ingredients
water, silica, adipic acid/diethylene glycol/glycerin crosspolymer, VP/hexadecene copolymer, dimethicone, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, glycerin, avena sativa (oat) kernel extract, squalane, ascorbyl palmitate, retinyl palmitate, tocopheryl acetate, BHT, cetyl dimethicone, bisabolol, dipotassium glycyrrhizate, glyceryl stearate, PEG-100 stearate, polysorbate 60, tetrasodium EDTA, butylene glycol, trimethylsiloxysilicate, xanthan gum, benzyl alcohol, isopropylparaben, isobutylparaben, butylparaben, phenoxyethanol, fragrance
- Other information
- Label
-
INGREDIENTS AND APPEARANCE
CVS HEALTH SPF 30 ULTRA SHEER
avobenzone, homosalate, octinoxate, octisalate, oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-118 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 70 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 20 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) DIMETHICONE (UNII: 92RU3N3Y1O) ISOPROPYLPARABEN (UNII: A6EOX47QK0) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) ASCORBYL PALMITATE (UNII: QN83US2B0N) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) PHENOXYETHANOL (UNII: HIE492ZZ3T) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) EDETATE SODIUM (UNII: MP1J8420LU) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) GLYCERYL 1-STEARATE (UNII: 258491E1RZ) SQUALANE (UNII: GW89575KF9) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) XANTHAN GUM (UNII: TTV12P4NEE) POLYSORBATE 60 (UNII: CAL22UVI4M) BUTYLPARABEN (UNII: 3QPI1U3FV8) WATER (UNII: 059QF0KO0R) OAT (UNII: Z6J799EAJK) ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S) (UNII: R9TPS68K19) VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9) GLYCERIN (UNII: PDC6A3C0OX) BENZYL ALCOHOL (UNII: LKG8494WBH) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) LEVOMENOL (UNII: 24WE03BX2T) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) PEG-100 STEARATE (UNII: YD01N1999R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-118-09 89 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/24/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/24/2017 Labeler - CVS Pharmacy (062312574)