Label: CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND SP- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 37808-182-08 - Packager: HEB
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 29, 2010
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- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- DIRECTIONS
- QUESTIONS OR COMMENTS
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INACTIVE INGREDIENTS
WATER, 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, 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, RED 4 (CI 14700), RED 33 (CI 17200), YELLOW 5 (CI 19140), METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND SP
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-182 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.3 mL in 100 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) GLYCERYL COCOATE (UNII: WVK1CT5994) GUAR GUM (UNII: E89I1637KE) EDETATE SODIUM (UNII: MP1J8420LU) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BENZYL ALCOHOL (UNII: LKG8494WBH) TRIETHYLENE GLYCOL (UNII: 3P5SU53360) POLIDOCANOL (UNII: 0AWH8BFG9A) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) MANGO (UNII: I629I3NR86) ALOE VERA LEAF (UNII: ZY81Z83H0X) SULISOBENZONE (UNII: 1W6L629B4K) HYPROMELLOSES (UNII: 3NXW29V3WO) 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:37808-182-08 236 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/30/2010 Labeler - HEB (007924756) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture