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 January 10, 2023

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  • Use

    Use: FDA Registered antiseptic for the care and cleaning of piercings.

  • 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.

  • WARNINGS:

    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.

  • ACTIVE INGREDIENTS

    ACTIVE INGREDIENTS: Benzalkonium Chloride 0.11%

  • OTHER INGREDIENTS

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

  • DISTRIBUTED BY

    DISTRIBUTED BY: Broadway Products LLC, Sellersburg, Indiana.

    LEARN MORE: www.drpiercing.com

    BARCODE XM001448MO3

    Dr. Piercing Afterca...roduct, 36 Swab Pierce New

  • Principal Display Label

    DR. PIERCING AFTERCARE™

    CLEAN, SOOTHES, PROTECTS

    36 Medication-filled Swabs Net 5.4mL

    MADE IN USA

    Aftercare Label

  • INGREDIENTS AND APPEARANCE
    DR. PIERCING AFTERCARE 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65734-504
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65734-504-3636 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 - Swabplus, L.P. (116984439)
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