Label: TOLNAFTATE ANTIFUNGAL- tolnaftate powder
- NDC Code(s): 57896-199-45
- Packager: Geri-Care Pharmaceuticals, Corp
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 8, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
-
DIRECTIONS
• shake well before use
• clean the affected area and dry thoroughly
• apply a thin layer of the product over affected area
twice daily (morning and night) or as directed by a doctor
• supervise children in the use of this product
• use daily for 4 weeks. If condition persists longer,
consult a doctor.For athlete's foot
• pay special attention to the spaces between the toes
• wear well-fitting ventilated shoes
• change shoes and socks at least once daily
• to prevent athlete’s foot, clean and dry feet thoroughly.
Apply as above once or twice daily.
This product is not effective on the scalp or nails. - Other Information
- INACTIVE INGREDIENTS
- PACKAGE LABEL
-
INGREDIENTS AND APPEARANCE
TOLNAFTATE ANTIFUNGAL
tolnaftate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57896-199 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 g Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) TALC (UNII: 7SEV7J4R1U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57896-199-45 45 g in 1 BOTTLE, DISPENSING; Type 7: Separate Products Requiring Cross Labeling 08/01/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 08/01/2011 Labeler - Geri-Care Pharmaceuticals, Corp (611196254) Registrant - GCP Laboratories (965480861) Establishment Name Address ID/FEI Business Operations GCP Laboratories 965480861 manufacture(57896-199)