ANTIFUNGAL FOOT TREATMENT- butenafine hydrochloride gel

Antifungal Foot Treatment by

Drug Labeling and Warnings

Antifungal Foot Treatment by is a Homeopathic medication manufactured, distributed, or labeled by Rida LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient                                                          

Butenafine hydrochloride 1%

Purpose

Antifungal

Uses

● cures most athlete's foot between the toes. Effectiveness on the bottom or sides of foot is unknown.
● relieves itching, burning, cracking, and scaling which accompany these conditions

Warnings

For external use only

Do not use

• on nails or scalp
•  in or near the mouth or the eyes
•  or vaginal yeast infections

• When using this productdo not get into the eyes. If eye contact occurs, rinse thoroughly with water.
• Stop use and ask a doctor iftoo much irritation occurs or irritation gets worse
• Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Directions

● adults and children 12 years and over:
      ● wash the affected skin with the soap and water and dry completly before applying.
      ● to open the applicator, twist the base to the ON position. Squeeze tube to dispence cream.

      ● for athlete's foot between the toes: apply to affected skin between and around the toes twice a day for 1 week (morning and night), or          once a day for 4 weeks, or as directed by a doctor. Wear well-fitting, ventilated shoes. Change shoes and socks at least once daily.

• Wipe applicator tip with a tissue and close the applicator by twisting the base to the OFF position
• wash hands after each use.

Childern under 12 years: ask a doctor

Other Information 

● store between 20º to 25º C (68º to 77º F)

Inactive ingredients

Tea Tree Oil, benzyl alcohol, cetyl alcohol, glycerin, glyceryl monostearate SE, polyoxyethylene (23) cetyl ether, propylene glycol dicaprylate, purified water, sodium benzoate, stearic acid, trolamine, white petrolatum

Product label

INGREDIENTS AND APPEARANCE

ANTIFUNGAL FOOT TREATMENT 
butenafine hydrochloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83004-016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BUTENAFINE HYDROCHLORIDE (UNII: R8XA2029ZI) (BUTENAFINE - UNII:91Y494NL0X)	BUTENAFINE HYDROCHLORIDE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
TEA TREE OIL (UNII: VIF565UC2G)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
CETETH-23 (UNII: 495CTZ441V)
PROPYLENE GLYCOL DICAPRYLATE (UNII: 581437HWX2)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
STEARIC ACID (UNII: 4ELV7Z65AP)
TROLAMINE (UNII: 9O3K93S3TK)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83004-016-01	1 in 1 CARTON	02/27/2025
1		20 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
unapproved homeopathic		02/27/2025

Labeler - Rida LLC (004425803)