Label: TOLNAFTATE- foot odor control powder spray aerosol, spray
- NDC Code(s): 68016-586-03
- Packager: Chain Drug Consortium, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
Flammable:
Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120ºF. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.
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Directions
- wash affected area and dry thoroughly
- shake can well and spray 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 conditions persist, consult a doctor
- to prevent athlete's foot, apply once or twice daily (morning and/or night)
- if nozzle clogs, clear under running water
- Other information
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
TOLNAFTATE
foot odor control powder spray aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-586 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 1.3 g in 113 g Inactive Ingredients Ingredient Name Strength DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) ISOBUTANE (UNII: BXR49TP611) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ALCOHOL (UNII: 3K9958V90M) SODIUM BICARBONATE (UNII: 8MDF5V39QO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68016-586-03 113 g in 1 CAN; Type 0: Not a Combination Product 06/01/2006 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 06/01/2006 Labeler - Chain Drug Consortium, LLC (101668460)