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Woodwards HandClens Foaming Sanitizer (Pacific Word Corporation)

Available Formats

Dosage Form Package Information Links
LIQUID 1800 mL in 1 BOTTLE, PUMP (60193-200-05) Label Information
LIQUID 50 mL in 1 BOTTLE, PUMP (60193-200-07) Label Information
LIQUID 236 mL in 1 BOTTLE, PUMP (60193-200-01) Label Information
LIQUID 1000 mL in 1 CARTRIDGE (60193-200-03) Label Information

Complete Woodwards HandClens Foaming Sanitizer Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active Ingredients

    Benzalkonium Chloride 0.13%


  • Purpose

    Antiseptic Sanitizer


  • Uses

    When soap and water are not available.

    Kills germs and helps prevent infections in minor cuts and abrasions.


  • WARNINGS

    Do not use in eyes,ears or mouth. In case of eye contact, flush with water immediately.

    Stop use and ask a doctor if rash or irritation occurs or if condition persists.

    Keep out of reach of children under 2 years of age.


  • Directions

    Apply as needed and rub into skin. No rinsing necessary.


  • Inactive Ingredients

    Water, Didecyldimonium Chloride, Fragrance, Methylparaben, Propylparaben, Propylene Glycol, Diazolidinyl Urea, Allantoin, Cocamidopropylamine Oxide, Cetrimonium Chloride, Cocamidopropyl Betaine, Green 5, Violet 2, Triethanolamine, Citric Acid


  • PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

    2 in 1
    Sanitizer & Lotion

    WOODWARD'S
    HandClens
    ®

    Foaming Sanitizer & Lotion

    Alcohol-Free Non-Flammable

    Softens Hands with Each Use!

    Kills 99.99%
    of Germs

    8 FL OZ (236 mL)

    Principal Display Panel - 236 mL Bottle Label

  • INGREDIENTS AND APPEARANCE
    WOODWARDS HANDCLENS FOAMING SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:60193-200
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    ALLANTOIN (UNII: 344S277G0Z)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:60193-200-01 236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2 NDC:60193-200-03 1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product
    3 NDC:60193-200-05 1800 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    4 NDC:60193-200-07 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part333A 06/03/2013
    Labeler - Pacific World Corporation (089693097)