Label: ORCHID BY H E B CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 37808-082-08 - Packager: H E B
- 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 August 1, 2014
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- ACTIVE INGREDIENT
- USES
- WARNINGS
- DIRECTIONS
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INACTIVE INGREDIENTS
WATER (AQUA), SODIUM LAURETH SULFATE, DISODIUM LAURETH SULFOSUCCINATE, COCAMIDOPROPYLAMINE OXIDE, GLYCERIN, SODIUM CHLORIDE, PEG-7 GLYCERYL COCOATE, GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE, TETRASODIUM EDTA, PROPYLENE GLYCOL, BENZYL ALCOHOL, FRAGRANCE (PARFUM), TRIETHYLENE GLYCOL, PPG-1-PEG-9 LAURYL GLYCOL ETHER, CEREUS GRANDIFLORUS (CACTUS) FLOWER EXTRACT, MANGIFERA INDICA (MANGO) FRUIT EXTRACT, ALOE BARBADENSIS LEAF JUICE, BENZOPHENONE-4, HYDROXYPROPYL METHYLCELLULOSE, CITRIC ACID, RED 4 (CI 14700), RED 33 (CI 17200), YELLOW 5 (CI 19140), METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE
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INGREDIENTS AND APPEARANCE
ORCHID BY H E B CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-082 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) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHLORIDE (UNII: 451W47IQ8X) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) EDETATE SODIUM (UNII: MP1J8420LU) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BENZYL ALCOHOL (UNII: LKG8494WBH) TRIETHYLENE GLYCOL (UNII: 3P5SU53360) PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) MANGO (UNII: I629I3NR86) ALOE VERA LEAF (UNII: ZY81Z83H0X) SULISOBENZONE (UNII: 1W6L629B4K) HYPROMELLOSES (UNII: 3NXW29V3WO) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) FD&C RED NO. 4 (UNII: X3W0AM1JLX) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-082-08 236 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 07/31/2014 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(37808-082)