Label: MED NAP CLEANSING TOWELETTE- benzalkonium chloride liquid

  • NDC Code(s): 0924-0243-00, 0924-0243-01
  • Packager: Acme United Corporation
  • 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 March 1, 2022

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  • Drug Facts Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    First Aid antiseptic

  • Use:

    First Aid antiseptic to help prevent infection in minor

    •cuts
    •scrapes
    •burns

  • Caution:

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control center right away.

  • Warnings

    For external use only

    Do not use ▪in the eyes ▪over large areas of the body •longer than 1 week

  • Stop use

    Stop use and ask doctor if the condition persists or gets worse

  • ASK DOCTOR

    Ask doctor before use if you have

    •deep or puncture wounds
    •animal bites
    •serious burns

  • Directions

    To open: Tear packet open at notch, remove towelette, use it only once

    •Clean affected area
    •Apply 1 to 3 times daily
    •May be covered with a sterile bandage, once area dries

  • Other Information

    Store at room temperature

  • Inactive Ingredients

    isopropyl alcohol, methylchloroisothiazolinone/methylisothiazolinone mixture, water

  • QUESTIONS

    Questions? 1.800.835.2263

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    MED NAP CLEANSING TOWELETTE 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0243
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.0018 mg  in 1.35 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0924-0243-001.35 mL in 1 PACKET; Type 0: Not a Combination Product03/02/2022
    2NDC:0924-0243-01100 in 1 BOX03/02/2022
    21.35 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/02/2022
    Labeler - Acme United Corporation (001180207)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation117825595manufacture(0924-0243)
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