Label: BLISTEX ODOR-EATERS POWDER- tolnaftate spray
- NDC Code(s): 10157-4645-1, 10157-4645-2
- Packager: Blistex Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in liquid)
- Purpose
- Uses
- Warnings
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Directions
- Shake container well before use.
- To prevent athlete's foot, wash the feet and dry thoroughly. Holding can 8" from the skin, spray a thin layer of the product on the feet once or twice daily (morning and/or night). Supervise children in the use of this product. Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.
- Wash hands after use.
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL - 113 g Can Label
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INGREDIENTS AND APPEARANCE
BLISTEX ODOR-EATERS POWDER
tolnaftate sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10157-4645 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 ISOBUTANE (UNII: BXR49TP611) SODIUM BICARBONATE (UNII: 8MDF5V39QO) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10157-4645-1 113 g in 1 CAN; Type 0: Not a Combination Product 12/09/2013 2 NDC:10157-4645-2 151 g in 1 CAN; Type 0: Not a Combination Product 11/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M005 12/09/2013 Labeler - Blistex Inc (005126354) Establishment Name Address ID/FEI Business Operations Blistex Inc 005126354 MANUFACTURE(10157-4645)