Home > Drugs A-Z > CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND SP

CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND SP (HEB)

Available Formats

Dosage Form Package Information Links
LIQUID 236 mL in 1 BOTTLE (37808-182-08) Label Information

Complete CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND SP Information

  • ACTIVE INGREDIENT

    TRICLOSAN 0.3 PERCENT


  • PURPOSE

    ANTIBACTERIAL


  • USES

    FOR WASHING TO REDUCE BACTERIA ON THE SKIN.


  • WARNINGS

    FOR EXTERNAL USE ONLY.

    WHEN USING THIS PRODUCT

    AVOID CONTACT WITH EYES.  IF CONTACT OCCURS, RINSE WITH WATER.

    STOP USING THIS PRODUCT AND ASK DOCTOR IF

    IRRITATION OR REDNESS DEVELOPS AND LASTS.

    KEEP OUT OF REACH OF CHILDREN

    IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.


  • DIRECTIONS

    APPLY ONTO DRY HANDS, WORK INTO RICH FOAMY LATHER, RINSE AND DRY THOROUGHLY.


  • QUESTIONS OR COMMENTS

    1-866-695-3030


  • 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.


  • INGREDIENTS AND APPEARANCE
    CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND SP 
    triclosan liquid
    Product 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