Drug Facts

Active Ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses

For the cure of most ringworm (tinea orporis) and athletes foot (tinea pedis) fungal infections. For the relief of itching; burning; scaling; cracking; redness; soreness; irritation; discomfort that may accompany fungal infections.

Warnings

For external use only.

Do not use

on children unless directed by a doctor.

When using this product

avoid eye contact. If eye contact occurs, rinse thoroughly with water for 10-15 minutes.

Stop use and ask a doctor if

if irritation occurs
no improvement is seen 4 weeks.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Consult a physician

before beginning treatment if pregnant/breast feeding.

Directions

Clean affected area with soap and water, rinse and dry thoroughly.
Apply to affected areas twice daily (morning and night) or as directed by physician.
Supervise children in the use of the product.
For athlete's foot: Pay special attention to spaces between the toes.
For athlete's foot and ringworm: Use daily for 4 weeks. If condition persists longer, consult physician.
Formula will dry completely in several minutes without residue.
Change socks regularly at least once a daily.
Wear well-fitted, ventilated shoes.

Inactive ingredients

Dimethyl Sulfoxide (DMSO), Green Tea Extract, Ascorbic Acid (Vitamin C), Povidone Iodine, Vitamin E Acetate

Questions:

call 1-800-748-6539

PROFESSIONAL DISPENSED ONLY BY PHYSICIANS CIDACIN Antifungal Treatment PROFESSIONAL Advanced Antifungal Solution 15mL / 0.5 oz Distributed by Pedicis Research LLC Radnor, PA 19087 Patent Pending

CIDACIN Antifungal Treatment 15ml (51151-000-01)

CIDACIN

CIDACIN BOX

CIDACIN ANTIFUNGAL TREATMENT
tolnaftate solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:51151-000
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
POVIDONE-IODINE (UNII: 85H0HZU99M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:51151-000-01	1 in 1 CARTON	02/05/2017
1		15 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M005	06/07/2012

Labeler - Pedicis Research LLC (078496974)