- Active ingredients
- Purpose
- Uses
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- 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 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
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
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
-
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 01/12/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/12/2017 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(69842-113)