Home > Drugs A-Z > WHITE LAVENDAR AND MINT ANTIBACTERIAL GENTLE FOAMING HAND SP

WHITE LAVENDAR AND MINT ANTIBACTERIAL GENTLE FOAMING HAND SP (HEB)

Available Formats

Dosage Form Package Information Links
LIQUID 236 mL in 1 BOTTLE (37808-181-08) Label Information

Complete WHITE LAVENDAR AND MINT ANTIBACTERIAL GENTLE FOAMING HAND SP Information

  • 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, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER/LEAF/STEM EXTRACT, MENTHA PIPERITA (PEPPERMINT) LEAF EXTRACT, ALOE BARBADENSIS LEAF JUICE, BENZOPHENONE-4, HYDROXYPROPYL METHYLCELLULOSE, EXT VIOLET 2 (CI 60730), RED 33 (CI 17200), METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE.


  • ACTIVE INGREDIENT

    TRICLOSAN 0.3 PERCENT


  • INGREDIENTS AND APPEARANCE
    WHITE LAVENDAR AND MINT ANTIBACTERIAL GENTLE FOAMING HAND SP 
    triclosan liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-181
    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)  
    LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)  
    MENTHA PIPERITA LEAF (UNII: A389O33LX6)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:37808-181-08 236 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