Label: ANTISEPTIC- benzethonium chloride solution
- NDC Code(s): 66977-032-08
- Packager: MPM Medical, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 17, 2024
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- Active Ingredient
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Warnings
For external use only. Keep out of reach of children.
This product is not for use on wild or domestic animal bites. If you have an animal bite, consult your physician immediately.
Do not use this product for more than 10 days. If condition worsens or persists, see your physician.
Do not bandage tightly.
If swallowed, get medical help or contact a Poison Control Center right away.
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INGREDIENTS AND APPEARANCE
ANTISEPTIC
benzethonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66977-032 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 1 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) POLOXAMER 188 (UNII: LQA7B6G8JG) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66977-032-08 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/1997 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 06/01/1997 Labeler - MPM Medical, LLC (081241522)