ANTIFUNGAL FOOT- tolnaftate aerosol, spray

ANTIFUNGAL FOOT by

Drug Labeling and Warnings

ANTIFUNGAL FOOT by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Use

cures most athlete's foot (tinea pedis) and ringworm (tinea corporis)
if used daily, can prevent recurrence of athlete's foot
relieves symptoms of athlete's foot, including, burning and cracking

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately. Do not use on children under 2 years of age unless directed by a doctor.

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

store between 68° to 77°F (20° to 25°C)

Questions/Comments?

1-855-345-5575

Inactive ingredients

butane, propane, alcohol, butylated hydroxytoluene, Zea Mays Starch.

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 08817

NO CFCs
CONTAINS NO CFCs WHICH DEPLETE THE OZONE LAYER

Made in China

Packaging

INGREDIENTS AND APPEARANCE

ANTIFUNGAL FOOT 
tolnaftate aerosol, spray

Product 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)