Label: 1200 WET WIPES- benzalkonium chloride cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by 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 July 13, 2020

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  • Active ingredients

    Benzalkonium Chloride 0.10%

  • Purpose

    Sanitizing

  • Use

    hand sanitizer to decrease bacteria on the skin.

  • Warnings

    For external use only. 

    Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.

    Do not use if you are allergic to any of the ingredients.

    Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.

    Keep out of reach of children unless under adult supervision. 

    If swallowed, get medical help

  • DOSAGE & ADMINISTRATION

    Direction

    Wet hands thoroughly with product and allow to dry without wiping.

  • Additional Information:

    • Store below 110°F (43°C).

    • May discolor certain fabrics or surfaces.

  • Inactive ingredients

    Sodium Carboxymethyl Lauryl Glucoside, Sodium PCA, Cocamide DEA, Citric Acid, Parfum / Fragrance, Ethyl glycerin, Vitamin E, Water, Aloe Essence Extract, Phenoxyethanol

  • SPL UNCLASSIFIED SECTION

    Distributed by DD Office Products, Inc.

    Los Angeles, CA | www.libertypp.com

    Made in China

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    1200 WET WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77081-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77081-001-121200 in 1 BAG07/15/2020
    13.5 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/15/2020
    Labeler - D D Office Products, Inc. (023854701)
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