Label: BENZALKONIUM CHLORIDE ANTISEPTIC TOWELETTE swab

  • 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 October 14, 2021

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

View All Sections
  • Active Ingredients

    Benzalkonium Chloride

  • Purpose

    Antiseptic

  • Use

    First aid antiseptic to help prevent skin infection in minor cuts, scrapes and burns

  • Warnings

    For external use only

  • Do Not Use

    • as a first aid antiseptic for more than 1 week
    • in the eyes
    • over large areas of the body
  • Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns


    Stop use if

    • irritation and redness develop
    • if condition persists for more than 72 hours, consult a physician
  • Keep out of reach of children.

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

  • Directions

    • clean affected area
    • apply 1 to 3 times daily
    • may be covered with a sterile bandage
    • if bandaged let dry first
  • Other Information

    stor at room temperaturel15°-30° C (59°-86° F)

  • Inactive ingredient

    purified water

  • RapidCare - Benzalkonium Chloride Antiseptic Wipes - 1pc

    Benzalkonium Chloride Antiseptic Wipes

  • INGREDIENTS AND APPEARANCE
    BENZALKONIUM CHLORIDE ANTISEPTIC TOWELETTE 
    benzalkonium chloride antiseptic towelette swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73659-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73659-003-011 in 1 PACKET; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/01/2020
    Labeler - Rapid Care, Inc (877432778)
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!