Label: CVS HEALTH SPF 30 OIL FREE SUN- avobenzone, homosalate, octinoxate, octisalate stick
- NDC Code(s): 69842-113-01
- 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 9, 2022
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask doctor if
- 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 - Other information
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Inactive ingredients
paraffin, C12-15 alkyl benzoate, ozokerite, butyloctyl salicylate, euphorbia cerifera (candililla) wax, neopentyl glycol, diethylhexanoate, beeswax, cyclopentasiloxane, ethylhexyl methoxycrylene, polyethylene, cetyl alcohol, polysilicone-11, dimethicone, tocopheryl acetate, ascorbyl palmitate, retinyl palmitate, BHT, neopentyl glycol diisostearate, propylparaben, fragrance
- Label
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INGREDIENTS AND APPEARANCE
CVS HEALTH SPF 30 OIL FREE SUN
avobenzone, homosalate, octinoxate, octisalate stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-113 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 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 20 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ASCORBYL PALMITATE (UNII: QN83US2B0N) DIMETHICONE (UNII: 92RU3N3Y1O) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) CETYL ALCOHOL (UNII: 936JST6JCN) PARAFFIN (UNII: I9O0E3H2ZE) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) CERESIN (UNII: Q1LS2UJO3A) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CANDELILLA WAX (UNII: WL0328HX19) NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW) YELLOW WAX (UNII: 2ZA36H0S2V) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) PROPYLPARABEN (UNII: Z8IX2SC1OH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-113-01 13.3 g in 1 PACKAGE; Type 0: Not a Combination Product 10/26/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 10/26/2015 Labeler - CVS Pharmacy (062312574)
