Fungus Master

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Fungus Master
Generic name
MICONAZOLE NITRATE
Manufacturer
Clinical Resolution Laboratory, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
36eb334e-246b-249f-e063-6294a90ab811
SPL ID
36eb334e-246c-249f-e063-6294a90ab811
Version
1
Effective date
2025-06-06
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:25:49
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings ■ Do not use on children under 2 years of age unless directed by a doctor. ■ For external use only. ■ Avoid contact with the eyes. ■ If irritation occurs or if there is no improvement within 4 weeks for the treatment of athlete's foot and ringworm, or 2 weeks for the treatment of jock itch, discontinue use and consult a doctor.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.