Label: TRIP 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 December 13, 2022

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  • Active ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antimicrobial

  • Uses

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

    For external use only

    When using this product

    avoid contact with eyes. In case of eye contact, flush eyes 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.

  • Directions

    • take wipe and rub thoroughly over all surfaces of both hands. Wet hands thoroughly with wipe
    • rub hands together briskly to dry without wiping
    • dispose of wipe
    • do not flush
  • Other information

    Store between 15°-30°C (59°F - 86°F).

    Avoid freezing and excessive heat above 40°C (104°F)

  • Inactive ingredients

    Purified Water, Aloe Barbadensis Leaf Extract, Citric Acid, Fragrance, Phenoxyethanol, Polysorbate 20, Potassium Sorbate, Sodium Benzoate, Vitamin E

  • Principal Display Panel

    TRIP WIPES 10CT

    73030-025-01

    ANTI-BACTERIAL WIPES

    SMELLS AMAZING • SOFTENS HANDS

    10 BIG WIPES

    KILLS 99.9% OF GERMS

    DO NOT FLUSH

  • INGREDIENTS AND APPEARANCE
    TRIP WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73030-025
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73030-025-0110 in 1 BOX12/13/2022
    11 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/13/2022
    Labeler - DETROIT WICK (061117661)
    Registrant - Precare Corp (858442403)
    Establishment
    NameAddressID/FEIBusiness Operations
    Precare Corp858442403manufacture(73030-025)
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