Label: MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC- benzalkonium chloride liquid

  • NDC Code(s): 0924-0246-00, 0924-0246-01, 0924-0246-02, 0924-0246-03, view more
    0924-0246-04, 0924-0246-05, 0924-0246-06
  • 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 February 22, 2023

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

View All Sections
  • Drug Facts Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    First Aid Antiseptic

  • Uses

    First Aid antiseptic to help prevent infection in minor

    •cuts
    •scrapes
    •burns

  • Warnings



    For External Use Only.

    Do not use

    •in the eyes
    •over large areas of the body
    •longer than 1 week

  • ASK DOCTOR

    Ask a doctor before use if you have •Deep or puncture wounds •Animal bites •Serious burns

  • Stop use

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

    .

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

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

  • 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

    methylchloroisothiazolinone/methylisothiazolinone mixture, water

  • QUESTIONS

    1.800.835.2263

  • PRINCIPAL DISPLAY PANEL

    Box Label Box Label

  • INGREDIENTS AND APPEARANCE
    MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0246
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0924-0246-001.35 mL in 1 PACKET; Type 0: Not a Combination Product02/11/2022
    2NDC:0924-0246-01100 in 1 BOX02/11/2022
    21.35 mL in 1 PACKET; Type 0: Not a Combination Product
    3NDC:0924-0246-021000 in 1 BOX02/11/2022
    31.35 mL in 1 PACKET; Type 0: Not a Combination Product
    4NDC:0924-0246-0312000 in 1 BOX02/11/2022
    41.35 mL in 1 PACKET; Type 0: Not a Combination Product
    5NDC:0924-0246-0420 in 1 BOX02/28/2023
    51.35 mL in 1 PACKET; Type 0: Not a Combination Product
    6NDC:0924-0246-0525 in 1 BOX02/28/2023
    61.35 mL in 1 PACKET; Type 0: Not a Combination Product
    7NDC:0924-0246-0660000 in 1 CONTAINER02/28/2023
    71.35 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 finalpart333E02/11/2022
    Labeler - Acme United Corporation (001180207)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation117825595manufacture(0924-0246)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!