Label: MED NAP OBSTETRICAL TOWELETTE- benzalkonium chloride liquid

  • NDC Code(s): 0924-0244-00, 0924-0244-01
  • 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 February 18, 2022

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

  • Use:

    Antiseptic cleansing of face, hands, and body without soap and water. Air dries in seconds.

  • 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

  • Stop use

    Stop use if irritation, redness, or other symptoms develop. Consult a doctor if the condition persists or gets worse.

  • Directions

    Tear open packet, unfold, and use as a washcloth.

  • Other Information

    •Store at room temperature

  • Inactive Ingredients

    chlorothymol, isopropyl alcohol, methylchloroisothiazolinone/methylisothiazolinone mixture, water

  • QUESTIONS

    Questions? 1.800.835.2263

  • PRINCIPAL DISPLAY PANEL

    Box Image Box Image

  • INGREDIENTS AND APPEARANCE
    MED NAP OBSTETRICAL TOWELETTE 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0244
    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)  
    CHLOROTHYMOL (UNII: LJ25TI0CVT)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0924-0244-001.35 mL in 1 PACKET; Type 0: Not a Combination Product02/25/2022
    2NDC:0924-0244-01100 in 1 BOX02/25/2022
    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 finalpart333E02/25/2022
    Labeler - Acme United Corporation (001180207)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation117825595manufacture(0924-0244)
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!