CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND SP (TRICLOSAN) LIQUID [HEB]

CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND SP (TRICLOSAN) LIQUID [HEB]
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NDC 37808-182-08
Set ID 99d9084b-97af-4f3b-b1f6-3acce1fb3799
Category HUMAN OTC DRUG LABEL
Packager HEB
Generic Name
Product Class
Product Number
Application Number PART333E
  • 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.

  • PRINCIPAL DISPLAY PANEL

    IMAGE OF CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND SOAP

  • INGREDIENTS AND APPEARANCE
    CACTUS FLOWER AND MANGO ANTIBACTERIAL GENTLE FOAMING HAND SP 
    triclosan liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-182
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.3 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37808-182-08236 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/30/2010
    Labeler - HEB (007924756)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOLLO HEALTH AND BEAUTY CARE201901209manufacture

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