Label: INVERNESS EAR CARE ANTISEPTIC- benzalkonium chloride solution
- NDC Code(s): 70094-010-02, 70094-010-04, 70094-010-08
- Packager: The Richline Group
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 17, 2025
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- Inverness EAR CARE ANTISEPTIC
- Active Ingredient
- Purpose
- INDICATIONS & USAGE
- Warnings
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Directions
For optimal results, follow these steps every day:
- Clean hands thoroughly with antibacterial soap before touching ears and earrings.
- Using cotton swab, cleanse front and back of ears 3 times a day with Ear Care Antiseptic. Gently rotate the earrings 2 or 3 times a day. DO NOT remove earrings.
- Keep hair, hair spray, shampoo, soap, cosmetics, perfume, etc. away from newly pierced ears. After shampooing, exercising, swimming, hot tubs, or use of any of the above products, rinse your ears in clear water and reapply Ear Care Antiseptic, (step 2), to your ears.
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Other Information
EAR LOBE PIERCING
- Leave earrings in your ears for 6 weeks.
- After 6 weeks the earrings may be removed; however, some type of post earring must be worn at all time during the first 6 months.
EAR CARTILAGE PIERCING
- Leave earrings in your ears for 12 weeks.
- After 12 weeks the earrings may be removed; however, some type of post earring must be worn at all times during the first year.
- Inactive Ingredient
- Questions?
- Representative Labeling
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INGREDIENTS AND APPEARANCE
INVERNESS EAR CARE ANTISEPTIC
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70094-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.2 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70094-010-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/04/2014 2 NDC:70094-010-02 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/04/2014 3 NDC:70094-010-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/04/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 06/04/2014 Labeler - The Richline Group (962801937)
