Label: INVERNESS EAR PIERCING- benzalkonium chloride kit

  • NDC Code(s): 70094-002-02, 70094-003-02
  • Packager: The Richline Group, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 8, 2023

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

  • Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.12% w/w

    Purpose

    Ear Care Antiseptic

  • Use

    for care of your pierced ears

  • Warnings

    • For external use only. Do not ingest. If swallowed, get medical help or contact Poison Control Center immediately.
    • In case of contact with eyes, flush with water.

    Keep out of reach of children.

    Stop use and ask a doctor

    if you experience pain, redenss, or swelling.

  • Directions

    For optimal results, follow these steps everday.

    • Clean hands thoroughly with antibacterial soap before touching ears and studs.
    • Using cotton swabs, cleanse front and back of ears 3 times a day with Ear Care Antiseptic. Gently rotate the studs 2 or 3 times a day. DO NOT remove earrings.
    • Keep hair, hair spray, shampoo, soap, cosmetics, perfume, ets. away from newly pierced ears. After shampooing, exercising, swimming, hot tubs, or use of any of the above products, rinse yours ears in clear water and reapply Ear Care Antiseptic
  • Inactive Ingredients

    Purified Water

  • Questions?

    Call 1-800-255-8556

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    INVERNESS EAR PIERCING 
    benzalkonium chloride kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70094-002
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70094-002-021 in 1 KIT01/01/2020
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE 60 mL
    Part 1 of 1
    HYGIENIC EAR CARE ANTISEPTIC 
    benzalkonium chloride solution
    Product Information
    Item Code (Source)NDC:70094-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.2 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70094-003-0260 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2020
    Labeler - The Richline Group, Inc. (962801937)