Label: CR-371059 TOLNAFTATE 1% CREAM cream
- NDC Code(s): 0536-1315-43
- Packager: Rugby Laboratories
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 28, 2023
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
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Directions
• Wash affected area and dry thoroughly
• Apply a thin layer over affected area twice daily (morning and night)
• Supervise children in the use of this product
• For athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes and change shoes and socks
at least once daily
• Use daily for 4 weeks; if condition persists longer, ask a doctor
• To prevent athlete's foot, apply once or twice daily (morning and/or night)
- Other Information
- Inactive Ingredients
- Questions and Comments?
- Label
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INGREDIENTS AND APPEARANCE
CR-371059 TOLNAFTATE 1% CREAM
cr-371059 tolnaftate 1% cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0536-1315 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 CETETH-20 (UNII: I835H2IHHX) MINERAL OIL (UNII: T5L8T28FGP) CHLOROCRESOL (UNII: 36W53O7109) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956) PETROLATUM (UNII: 4T6H12BN9U) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) Product Characteristics Color Score Shape FREEFORM Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0536-1315-43 1 g in 1 BOX; Type 0: Not a Combination Product 03/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 03/01/2021 Labeler - Rugby Laboratories (079246066)