- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- DIRECTIONS
- QUESTIONS OR COMMENTS
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INACTIVE INGREDIENTS
WATER, SODIUM LAURETH SULFATE, ACRYLATES COPOLYMER, COCAMIDOPROPYL BETAINE, COCAMIDE DEA, SODIUM CHLORIDE, FRAGRANCE, ALOE BARBADENSIS LEAF JUICE, PEG-7 GLYCERYL COCOATE, HELIANTHUS ANNUUS (SUNFLOWER) EXTRACT, CEREUS GRANDIFLORUS (CACTUS) FLOWER EXTRACT, MANGIFERA INDICA (MANGO) FRUIT EXTRACT, POLYETHYLENE, TETRASODIUM EDTA, SODIUM STYRENE/PEG-10 MALEATE/NONOXYNOL-10 MALEATE/ACRYLATES COPOLYMER, AMMONIUM NONOXYNOL-4 SULFATE, CITRIC ACID, SODIUM HYDROXIDE, MANNITOL, CELLULOSE, HYDROXYPROPYL METHYLCELLULOSE, MICA, TITANIUM OXIDE (CI 77891), IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), YELLOW 5 (CI 19140), RED 4 (CI 14700), RED 33 (CI 17200), METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CACTUS FLOWER AND MANGO ANTIBACTERIAL DEEP CLEANSING HAND SP
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-291 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) CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) COCO DIETHANOLAMIDE (UNII: 92005F972D) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERYL COCOATE (UNII: WVK1CT5994) HELIANTHUS ANNUUS FLOWER (UNII: BKJ0J3D1BP) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) MANGO (UNII: I629I3NR86) LOW DENSITY POLYETHYLENE (UNII: J245LN42AI) EDETATE SODIUM (UNII: MP1J8420LU) NONOXYNOL-10 (UNII: K7O76887AP) AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SODIUM HYDROXIDE (UNII: 55X04QC32I) MANNITOL (UNII: 3OWL53L36A) POWDERED CELLULOSE (UNII: SMD1X3XO9M) HYPROMELLOSES (UNII: 3NXW29V3WO) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 4 (UNII: X3W0AM1JLX) D&C RED NO. 33 (UNII: 9DBA0SBB0L) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-291-08 236 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