Label: DR. PIERCING AFTERCARE- benzalkonium chloride 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 July 29, 2023

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

View All Sections
  • ACTIVE INGREDIENTS

    Benzalkonium Chloride 0.11%

  • Purpose

    Antiseptic

  • Use

    FDA Registered antiseptic for the care and cleaning of piercings.

  • WARNINGS:

    For external use only.If redness, irritation, infection or swelling occurs, discontinue use and consult a physician. Keep out of eyes. Do not insert into the ear canal. Store at room temprature.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • Directions:

    1. Hold swab with the colored round marker end up.

    2. Bend the colored round marker tip until it "snaps".

    3. Liquid flows down into the white tip.

    4. Apply medicated tip to piercing. Dispose.

  • OTHER INGREDIENTS

    Isotonic Saline Solution, Aloe Vera, Allantoin, Panthenol/Pro-Vitamin B5.

  • PRINCIPAL DISPLAY PANEL

    Aftercare Label

  • INGREDIENTS AND APPEARANCE
    DR. PIERCING AFTERCARE 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81926-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    CUPRIC NITRATE (UNII: 9TC879S2ZV)  
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ALLANTOIN (UNII: 344S277G0Z)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81926-001-3636 in 1 CASE01/01/2021
    10.15 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/2021
    Labeler - Broadway Products LLC (002672936)
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!