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OTC products · Product label record

Defense Antifungal Medicated Bar drug information

TOLNAFTATE
Defense Soap LLC · TOPICAL

Product NDC: 70856-3581

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameTOLNAFTATE
Labeler / manufacturerDefense Soap LLC
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC70856-3581
Label effective date2026-09-09

Official product label reference

Defense Antifungal Medicated Bar — Defense Soap LLC

This page contains 10 source sections for TOLNAFTATE, topical route. Label set 812d78ea-a14a-e3a2-e053-2a91aa0a6ff5, version 8.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses Proven clinically effective in the treatment of most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris). For effective relief of itching, burning and cracking skin.

Purpose

Purpose Antifungal
Dosage and administration — label text
Directions Wash affected area well and let product sit 1-2 minutes before rinsing. Make sure to dry affected area thoroughly. Supervise children in the use of this product. For Athlete's foot: pay special attention to the spaces between the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily. Use 1-2 times daily. Use daily for 4 weeks; if condition persists longer, ask a doctor. This product is not effective on the scalp or nails.
Warnings
Warnings For external use only When using this product When using this product avoid contact with the eye Stop use and ask a doctor if Stop use and ask a doctor if irritation occurs or if there is no improvement within 2 weeks for jock itch or within 4 weeks for athlete's foot and ringworm. Do not use Do Not use on children under 2 under of age except under the advice and supervision of a doctor. Keep out of reach of children. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Active ingredient
Active ingredient Tolnaftate 1%
While using this medicine
When using this product When using this product avoid contact with the eye
When to stop use and seek help
Stop use and ask a doctor if Stop use and ask a doctor if irritation occurs or if there is no improvement within 2 weeks for jock itch or within 4 weeks for athlete's foot and ringworm.
Do not use
Do not use Do Not use on children under 2 under of age except under the advice and supervision of a doctor.
Child safety
Keep out of reach of children. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Inactive ingredient
Inactive ingredients Sodium Palmate, Sodium Palm Kernelate, Water, Glycerin, Sodium Gluconate, Eucalyptus Globulus Leaf Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Palm Acid, Sodium Chloride, Palm Kernel Acid, Charcoal Powder

Official sources and product identifiers

Substances listed: TOLNAFTATE

RxNorm identifiers: 1807715

Package NDC codes

70856-3581-3

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.