Label: COVERGIRL TRUBLEND BASE BUSINESS EVERYDAY DEFENSE PRIMER SPF 20- ensulizole liquid
- NDC Code(s): 22700-157-01
- Packager: NOXELL CORPORATION
- 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 January 24, 2023
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- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
- Directions
- Other information
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INACTIVE INGREDIENT
Aqua/Water/Eau, Cyclopentasiloxane, Talc, Propylene Glycol, Dimethicone, Aluminum Starch Octenylsuccinate, PEG/PPG-18/18 Dimethicone, Sodium Chloride, PVP, Phenoxyethanol, Sodium Hydroxide, Ethylene/Methacrylate Copolymer, Synthetic Beeswax, Trihydroxystearin, Methicone, 1,2-Hexanediol, Caprylyl Glycol, Silica, Sodium Benzoate, Synthetic Wax, Polyglyceryl-4 Isostearate, Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Isopropyl Titanium Triisostearate, Ethylene Brassylate, Polyethylene.
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INGREDIENTS AND APPEARANCE
COVERGIRL TRUBLEND BASE BUSINESS EVERYDAY DEFENSE PRIMER SPF 20
ensulizole liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:22700-157 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE 3 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM BENZOATE (UNII: OJ245FE5EU) ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD) TALC (UNII: 7SEV7J4R1U) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) HEXYL LAURATE (UNII: 4CG9F9W01Q) DIMETHICONE (UNII: 92RU3N3Y1O) TRIHYDROXYSTEARIN (UNII: 06YD7896S3) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CAPRYLYL GLYCOL (UNII: 00YIU5438U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:22700-157-01 30 mL in 1 TUBE; Type 0: Not a Combination Product 03/28/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 03/28/2019 Labeler - NOXELL CORPORATION (003082997) Establishment Name Address ID/FEI Business Operations NOXELL CORPORATION 003082997 manufacture(22700-157)