Label: CIDACIN ANTIFUNGAL TREATMENT- tolnaftate solution
- NDC Code(s): 51151-000-01
- Packager: Pedicis Research LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 5, 2023
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- Drug Facts
- Active Ingredient
- Purpose
- Uses
- Warnings
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Directions
- Clean affected area with soap and water, rinse and dry thoroughly.
- Apply to affected areas twice daily (morning and night) or as directed by physician.
- Supervise children in the use of the product.
- For athlete's foot: Pay special attention to spaces between the toes.
- For athlete's foot and ringworm: Use daily for 4 weeks. If condition persists longer, consult physician.
- Formula will dry completely in several minutes without residue.
- Change socks regularly at least once a daily.
- Wear well-fitted, ventilated shoes.
- Inactive ingredients
- Questions:
- PRINCIPAL DISPLAY PANEL
- CIDACIN Antifungal Treatment 15ml (51151-000-01)
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INGREDIENTS AND APPEARANCE
CIDACIN ANTIFUNGAL TREATMENT
tolnaftate solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51151-000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 1 g in 100 mL Inactive Ingredients Ingredient Name Strength DIMETHYL SULFOXIDE (UNII: YOW8V9698H) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ASCORBIC ACID (UNII: PQ6CK8PD0R) POVIDONE-IODINE (UNII: 85H0HZU99M) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51151-000-01 1 in 1 CARTON 02/05/2017 1 15 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 Drug M005 06/07/2012 Labeler - Pedicis Research LLC (078496974)