Label: AGAVE CACTUS LIGHT- dimethicone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 76214-004-01 - Packager: SKINFOOD CO., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 July 15, 2011
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
WATER, AGAVE TEQUILANA LEAF EXTRACT, CYCLOPENTASILOXANE, ALCOHOL DENAT., ARBUTIN, BUTYLENE GLYCOL, LECITHIN, DIMETHICONE CROSSPOLYMER, BETAINE, CEREUS GRANDIFLORUS (CACTUS) FLOWER EXTRACT, TRIETHANOLAMINE, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, CARBOMER, LACTOBACILLUS FERMENT LYSATE FILTRATE, HYDROLYZED VIOLA TRICOLOR EXTRACT, BISABOLOL, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, MAACKIA FAURIEI STEM EXTRACT, PALMITOYL OLIGOPEPTIDE, ADENOSINE, POLYSORBATE 20, GLYCERIN, PROPYLENE GLYCOL, GLYCERYL POLYMETHACRYLATE, PALMITOYL PENTAPEPTIDE-4, DISODIUM EDTA, PALMITOYL TETRAPEPTIDE-7, HYDROGENATED LECITHIN, CHOLESTEROL, DIPOTASSIUM GLYCYRRHIZATE, METHYLPARABEN, PROPYLPARABEN, PHENOXYETHANOL, FRAGRANCE
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AGAVE CACTUS LIGHT
dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76214-004 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 0.45 g in 45 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) AGAVE TEQUILANA LEAF (UNII: 05545M0E3M) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ARBUTIN (UNII: C5INA23HXF) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) BETAINE (UNII: 3SCV180C9W) PHENOXYETHANOL (UNII: HIE492ZZ3T) TROLAMINE (UNII: 9O3K93S3TK) METHYLPARABEN (UNII: A2I8C7HI9T) MAACKIA FLORIBUNDA STEM (UNII: 84UXW52K8Y) PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C) ADENOSINE (UNII: K72T3FS567) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYSORBATE 20 (UNII: 7T1F30V5YH) GLYCERIN (UNII: PDC6A3C0OX) EDETATE DISODIUM (UNII: 7FLD91C86K) PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) CHOLESTEROL (UNII: 97C5T2UQ7J) PROPYLPARABEN (UNII: Z8IX2SC1OH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76214-004-01 45 g in 1 CARTON Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 03/01/2011 Labeler - SKINFOOD CO., LTD. (690324173) Registrant - SKINFOOD CO., LTD. (690324173) Establishment Name Address ID/FEI Business Operations SKINFOOD CO., LTD. 690324173 manufacture
