Label: TOLNAFTATE cream
- NDC Code(s): 0904-0722-36
- Packager: Major Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- clean the affected area and dry thoroughly
- apply a thin layer of the product over the affected area twice daily (morning and night) or as directed by a doctor
- supervise children in the use of this product
For athlete's foot
- use daily for 4 weeks. If condition persists longer, consult a doctor
- pay special attention to the spaces between the toes
- wear well fitting ventilated shoes
- change shoes and socks at least once daily
For ringworm, use daily for 4 weeks. If condition persists longer, consult a doctor.
For jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor.
This product is not effective on the scalp or nails.
- Other information
- Inactive ingredients
- Questions?
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Principal Display Panel – 0.5 oz Tube
MAJOR® *Compare to Active Ingredient of Tinactin®
NDC 0904-0722-36
Antifungal
Cream (Tolnaftate 1%) N309040722362
CURES ATHLETE'S FOOT, *This product is not manufactured or
JOCK ITCH AND RINGWORM distributed by Schering-Plough Healthcare
Relives Burning and Itching Products, Inc. owner of the registered
• Odorless • Greaseless • Non-Staining trademark, Tinactin®
Net Wt. 0.5 OZ (14.18 g)
- Principal Display Panel – 0.5 oz Carton
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INGREDIENTS AND APPEARANCE
TOLNAFTATE
tolnaftate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0904-0722 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETETH-20 (UNII: I835H2IHHX) CHLOROCRESOL (UNII: 36W53O7109) MINERAL OIL (UNII: T5L8T28FGP) PETROLATUM (UNII: 4T6H12BN9U) SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0904-0722-36 1 in 1 CARTON 02/11/2010 1 14.18 g in 1 TUBE; 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 02/11/2010 Labeler - Major Pharmaceuticals (191427277)