NDC | 69842-132-22 |
Set ID | 63f0cf27-9355-097d-e053-2a91aa0a3c50 |
Category | HUMAN OTC DRUG LABEL |
Packager | CVS Pharmacy |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- 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, Propylene Glycol, Styrene/Acrylates Copolymer, Behenyl Alcohol, Glyceryl Stearate, Microcrystalline Cellulose, Benzyl Alcohol, Diethylhexyl Syringylidenemalonate, Palmitic Acid, Myristyl Alcohol, Stearic Acid, Hydrolyzed Wheat Protein/PVP Crosspolymer, Lauryl Alcohol, Cetyl Alcohol, Retinyl Palmitate (Vitamin A Palmitate), Tocopherol (Vitamin E), Sodium Ascorbyl Phosphate (Vitamin C Phosphate), Lecithin, Cellulose Gum, Caprylic/Capric Triglyceride, Chlorphensin, Fragrance, Butylated PVP, Disodium EDTA
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CVS HEALTH ULTRA PROTECTION SPF 100
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-132 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 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 PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TOCOPHEROL (UNII: R0ZB2556P8) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) WATER (UNII: 059QF0KO0R) STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) DOCOSANOL (UNII: 9G1OE216XY) BENZYL ALCOHOL (UNII: LKG8494WBH) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) STEARIC ACID (UNII: 4ELV7Z65AP) PALMITIC ACID (UNII: 2V16EO95H1) LAURYL ALCOHOL (UNII: 178A96NLP2) MYRISTYL ALCOHOL (UNII: V42034O9PU) CETYL ALCOHOL (UNII: 936JST6JCN) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) CHLORPHENESIN (UNII: I670DAL4SZ) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-132-22 177 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/29/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/29/2018 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(69842-132)