Label: BOA VIDA CANOPY- dimethicone cream
- NDC Code(s): 62654-144-04, 62654-144-05
- Packager: Central Solutions Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 9, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive Ingredients
Water, Polyglyceryl-4 Isostearate, Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate,Cyclotetrasiloxane, Cyclopentasiloxane, Mineral Oil, Isopropyl Palmitate, Ethylhexyl Palmitate, Theobroma Grandiflorum Seed (Cupuacu Butter), Glycerin, Cetyl Dimethicone, Tocopherol (Vitamin E), Beeswax, Diazolidinyl Urea, Hydrogenated Castor Oil, Retinyl Palmitate (Vitamin A), Cholecalciferol (Vitamin D3), Beeswax, Zea Mays Oil, Methyl Paraben, Fragrance, Sodium Chloride
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BOA VIDA CANOPY
dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62654-144 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) HEXYL LAURATE (UNII: 4CG9F9W01Q) QUADROSILAN (UNII: C5KT601WPM) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) MINERAL OIL (UNII: T5L8T28FGP) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) ETHYLHEXYL PALMITATE (UNII: 2865993309) THEOBROMA GRANDIFLORUM SEED (UNII: Q7RNT1G37V) GLYCERIN (UNII: PDC6A3C0OX) TOCOPHEROL (UNII: R0ZB2556P8) YELLOW WAX (UNII: 2ZA36H0S2V) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) CHOLECALCIFEROL (UNII: 1C6V77QF41) CORN OIL (UNII: 8470G57WFM) METHYLPARABEN (UNII: A2I8C7HI9T) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62654-144-05 148 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/01/2011 2 NDC:62654-144-04 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/01/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 11/01/2011 Labeler - Central Solutions Inc (007118524) Establishment Name Address ID/FEI Business Operations Central Solutions Inc 007118524 manufacture(62654-144)