Home NDC 87885-001 MiratiFul Nail Fungus Treatment
Product NDC 87885-001
11-digit product format 878850001
Labeler code 87885
Product ID 87885-001_58295d84-4d47-3613-e063-6394a90a1fd6
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate
Dosage form SOLUTION
Route TOPICAL
Labeler Texas MiratiFul Enterprises Inc.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-03
Substance TOLNAFTATE
Active strength 1 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base MiratiFul Nail Fungus Treatment
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE 1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 06KB629TKV Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 313423 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 8 of 49 · 973 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87885-001-01 87885000101 15 mL in 1 BOTTLE, WITH APPLICATOR (87885-001-01) 15 ml 2026-08-03 No No Current