Label: ANTIFUNGAL FOOT- tolnaftate aerosol, spray
- NDC Code(s): 52000-418-03
- Packager: Universal Distribution Center LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 16, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Use
-
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 temperatures above 120°F (49°C).
When using this product • avoid contact eyes & face • use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
Stop use and ask a doctor if • irritation occurs • there is no improvement after 4 weeks
-
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 space between the toes; wear well-fitted, ventilated shoes and change shoes and socks at least once a day.
• use daily for 4 weeks; if condition persists longer, consult a doctor
• to prevent athlete's foot, apply once or twice daily (morning and night)
• in case of clogging, clean nozzle with a pin - Other Information
- Questions/Comments?
- Inactive ingredients
-
SPL UNCLASSIFIED SECTION
FOR ATHLETE'S FOOT
Cures & Prevents Most Athlete's Foot
Relieves Itching & Burning
Fights Odor All Day*Compare to the Active Ingredient in Tinactin®
CAUTION
CONTENTS UNDER PRESSURE
Read precautions on back panel.Distributed by:
UNIVERSAL DISTRIBUTION CENTER, LLC
Edison, NJ 08817NO CFCs
CONTAINS NO CFCs WHICH DEPLETE THE OZONE LAYERMade in China
- Packaging
-
INGREDIENTS AND APPEARANCE
ANTIFUNGAL FOOT
tolnaftate aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52000-418 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 BUTANE (UNII: 6LV4FOR43R) PROPANE (UNII: T75W9911L6) ALCOHOL (UNII: 3K9958V90M) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) STARCH, CORN (UNII: O8232NY3SJ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52000-418-03 103 g in 1 CAN; Type 0: Not a Combination Product 07/16/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 07/16/2024 Labeler - Universal Distribution Center LLC (019180459) Registrant - Universal Distribution Center LLC (019180459)
