Home NDC 72654-001 Fungus Master Antifungal Treatment
Product NDC 72654-001
11-digit product format 726540001
Labeler code 72654
Product ID 72654-001_4a6d1ee4-a8ad-861a-e063-6294a90a3423
Type HUMAN OTC DRUG
Nonproprietary name MICONAZOLE NITRATE
Dosage form LOTION
Route TOPICAL
Labeler Ebanel Laboratories, Inc
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-11-01
Substance MICONAZOLE NITRATE
Active strength 20 mg/mL
Pharmacologic classes Azole Antifungal [EPC], Azoles [CS]
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 Fungus Master Antifungal Treatment
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MICONAZOLE NITRATE 20 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination VW4H1CYW1K Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 998521 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72654-001-01 Fungus Master Antifungal Treatment 30 mL in 1 BOTTLE, WITH APPLICATOR LOTION 30 6 72654-001-02 Fungus Master Antifungal Treatment 59 mL in 1 BOTTLE, WITH APPLICATOR LOTION 59 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72654-001 FUNGUS MASTER ANTIFUNGAL TREATMENT (MICONAZOLE NITRATE) LOTION [EBANEL LABORATORIES, INC] 5 Current NDC, Legacy NDC, 2 package rows 20231227_f7b011b2-11e5-46f1-afed-89f438985e00.zip
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72654-001-01 72654000101 30 mL in 1 BOTTLE, WITH APPLICATOR (72654-001-01) 30 ml 2019-11-01 0000-00-00 No No Current 72654-001-02 72654000102 59 mL in 1 BOTTLE, WITH APPLICATOR (72654-001-02) 59 ml 2019-11-01 0000-00-00 No No Current