Label: BENGAMA ANTIFUNGAL- tolnaftate solution
- NDC Code(s): 69666-831-04
- Packager: Genuine Drugs
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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Drug Label Information
Updated February 17, 2023
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- Active ingredient (in each gram)
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INGREDIENTS AND APPEARANCE
BENGAMA ANTIFUNGAL
tolnaftate solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69666-831 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 1 mg in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69666-831-04 1 in 1 BOX 04/20/2015 1 118 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 04/20/2015 Labeler - Genuine Drugs (079610378)