Label: CVS HEALTH AGE DEFENSE SPF 70 FACE- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
- NDC Code(s): 69842-119-09, 69842-119-10
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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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- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
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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, styrene/acrylates copolymer, polysilicone-15, silica, beeswax, caprylyl methicone, cetyl dimethicone, dimethicone, ethylhexylglycerin, tocopheryl acetate, ascorbic acid, camellia sinensis leaf extract, retinyl palmitate, dipotassium glycyrrhizate, BHT, bisabolol, glyceryl stearate, PEG-100 stearate, sodium polyacrylate, acrylates/C12-22 alkyl methacrylate copolymer, ethylhexyl stearate, xanthan gum, trideceth-6, trimethylsiloxysilicate, disodium EDTA, methylisothiazolinone
- Other information
- Label
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INGREDIENTS AND APPEARANCE
CVS HEALTH AGE DEFENSE SPF 70 FACE
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-119 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 60 mg in 1 mL Inactive Ingredients Ingredient Name Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) DIMETHICONE (UNII: 92RU3N3Y1O) WHITE TEA (UNII: O0M3396E09) BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) EDETATE SODIUM (UNII: MP1J8420LU) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) GLYCERYL 1-STEARATE (UNII: 258491E1RZ) YELLOW WAX (UNII: 2ZA36H0S2V) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) XANTHAN GUM (UNII: TTV12P4NEE) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) WATER (UNII: 059QF0KO0R) POLYSILICONE-15 (UNII: F8DRP5BB29) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) TRIDECETH-6 (UNII: 3T5PCR2H0C) LEVOMENOL (UNII: 24WE03BX2T) PEG-100 STEARATE (UNII: YD01N1999R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-119-10 1 in 1 BOX 10/23/2015 1 NDC:69842-119-09 89 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 10/23/2015 Labeler - CVS Pharmacy (062312574)