Label: INVERNESS EAR CARE- benzalkonium chloride solution

  • NDC Code(s): 70094-007-01
  • Packager: The Richline Group, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 9, 2024

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

  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.12% w/w

    Purpose

    Antiseptic

  • Use

    First aid to prevent infection of 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, redness, or swelling.

  • Directions

    For optimal results, follow these steps daily:

    • Clean hands thoroughly with soap before touching ears or piercing studs.
    • Using a cotton swab saturated with Ear Care solution, cleanse front and back of piercing 3 time daily.
    • Gently rotate the earrings while cleasnsing.
    • DO NOT remove earrings.
    • Keep hair, hair spray, shampoo, soap, cosmetics, perfume, etc. away from newly pierced ears.
    • After shampooing, exercising, swimming, or use of hair products, rinse ears in clear water and reapply Ear Care Solution.
  • Inactive ingredients

    Purified Water

  • Questions?

    Call 1-800-255-8556

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    INVERNESS EAR CARE 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70094-007
    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:70094-007-01118 mL in 1 BOTTLE; Type 0: Not a Combination Product05/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/31/2024
    Labeler - The Richline Group, Inc. (962801937)