Label: SOFTSOAP  FOAMING HAND SANITIZER WITH LIGHT MOISTURIZERS- benzalkonium chloride liquid 

  • Label RSS
  • NDC Code(s): 35000-818-36
  • Packager: Colgate Palmolive Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 04/10

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

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  • Active Ingredient

    Benzalkonium Chloride 0.1%

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  • Purpose

    Anti-bacterial

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  • Uses

    • For hand sanitizing to decrease bacteria on the skin
    • Recommended for repeated use
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  • Warnings

    For external use only.

    When using this product avoid contact with eyes. In case of eye contact, flush with water.

    Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a poison Control Center right away.

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  • Directions

    • Pump a small amount of foam into palm of hand
    • Rub thoroughly over all surfaces of both hands
    • Rub hands together briskly until dry
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  • Inactive ingredients

    Water, dihydroxypropyl PEG-5, linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, aloe barbadensis leaf juice

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  • Questions? Comments?

    Call 1-800-432-8226

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  • SPL UNCLASSIFIED SECTION

    Dist. by:
    COLGATE-PALMOLIVE
    COMPANY
    COMMERCIAL CUSTOMER GROUP
    Morristown, NJ 07962-1928 USA

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  • PRINCIPAL DISPLAY PANEL - 1.25 L Label

    Softsoap®
    brand

    42.2 FL OZ (1.32 QT) 1.25 L

    PRINCIPAL DISPLAY PANEL - 1.25 L Label
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  • INGREDIENTS AND APPEARANCE
    SOFTSOAP   FOAMING HAND SANITIZER WITH LIGHT MOISTURIZERS
    benzalkonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:35000-818
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride 1.0 mL  in 1 L
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:35000-818-36 1.25 L in 1 BOTTLE, DISPENSING
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 04/26/2010
    Labeler - Colgate Palmolive Company (068693167)
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