Mycozyl AL

NDC 59088-443 · PURETEK CORPORATION

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameTolnaftate

Dosage formLIQUID

RouteTOPICAL

Active ingredient(s)TOLNAFTATE

Strength.1 g/10mL

Marketing categoryUNAPPROVED DRUG OTHER

Packages

59088-443-01 — 10 mL in 1 BOTTLE (59088-443-01)

59088-443-03 — 30 mL in 1 BOTTLE, WITH APPLICATOR (59088-443-03)

FDA lists these products with the same active ingredient.

56104-252 — Tolnaftate, 56104-902 — Tolnaftate, 57237-354 — Tolnaftate, 57896-199 — TOLNAFTATE, 58593-285 — Tolnaftate, 58593-286 — Tolnaftate, 58593-288 — Tolnaftate, 58593-800 — TOLNAFTATE, 59088-264 — Tolnaftate, Hydrocortisone, 59088-279 — Tolnaftate, Hydrocortisone, 59088-477 — Tolnaftate, 59088-640 — Tolnaftate, 59779-511 — Foot and Sneaker Spray, 60771-0040 — TOLNAFTATE, 62858-101 — TOLNAFTATE, 63347-511 — TOLNAFTATE, 63868-181 — Tolnaftate Powder Spray, 63868-798 — Antifungal Liquid Spray, 63941-540 — Tolnaftate Jock Itch Powder Spray - Talc Free, 63941-541 — Tolnaftate Athletes Foot Powder Spray Talc Free, +315 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.