Label: ORCHID BY H E B ANTIBACTERIAL MOISTURIZING VANILLA AND APPLE BLOSSOM- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 37808-071-08 - Packager: H E B
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 19, 2015
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENTS
WATER (AQUA), SODIUM LAURETH SULFATE, ACRYLATES COPOLYMER, GLYCOL DISTEARATE, COCAMIDOPROPYL BETAINE, MYRISTYL ALCOHOL, GLYCERIN, AMMONIUM CHLORIDE, GLYCERETH-26, COCO-GLUCOSIDE, GLYCERYL OLEATE, LAURYL LACTYL LACTATE, VANILL PLANIFOLIA FRUIT EXTRACT, PYRUS MALUS (APPLE) FRUIT EXTRACT, TOCOPHERYL ACETATE, BENZOPHENONE-4, DISODIUM EDTA, SODIUM HYDROXIDE, CITRIC ACID, BENZYL ALCOHOL, FRAGRANCE (PARFUM), MANNITOL, CELLULOSE, HYDROYXPROPYL METHYLCELLULOSE, RETINYL PALMITATE, IRON OXIDES (CI 77491), RED 33 (CI 17200), MICA (CI 77019), TITANIUM DIOXIDE (CI 77891), METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE
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INGREDIENTS AND APPEARANCE
ORCHID BY H E B ANTIBACTERIAL MOISTURIZING VANILLA AND APPLE BLOSSOM
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-071 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13) GLYCOL DISTEARATE (UNII: 13W7MDN21W) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) MYRISTYL ALCOHOL (UNII: V42034O9PU) GLYCERIN (UNII: PDC6A3C0OX) AMMONIUM CHLORIDE (UNII: 01Q9PC255D) GLYCERETH-26 (UNII: NNE56F2N14) COCO GLUCOSIDE (UNII: ICS790225B) GLYCERYL OLEATE (UNII: 4PC054V79P) LAURYL LACTATE (UNII: G5SU0BFK7O) VANILLA (UNII: Q74T35078H) APPLE (UNII: B423VGH5S9) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SULISOBENZONE (UNII: 1W6L629B4K) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM HYDROXIDE (UNII: 55X04QC32I) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) BENZYL ALCOHOL (UNII: LKG8494WBH) MANNITOL (UNII: 3OWL53L36A) POWDERED CELLULOSE (UNII: SMD1X3XO9M) HYPROMELLOSES (UNII: 3NXW29V3WO) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) FERRIC OXIDE RED (UNII: 1K09F3G675) D&C RED NO. 33 (UNII: 9DBA0SBB0L) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-071-08 236 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/18/2015 Labeler - H E B (007924756) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(37808-071)