FDA.reportPublic FDA data

RoyceDerm Anti-Fungal Cream

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
RoyceDerm Anti-Fungal Cream
Generic name
MICONAZOLE NITRATE 2%
Manufacturer
RoyceDerm LLC
Product type
HUMAN OTC DRUG
SPL set ID
4e861073-88e8-b2f7-e063-6394a90ab94a
SPL ID
4e861073-88e9-b2f7-e063-6394a90ab94a
Version
1
Effective date
2026-04-02
Source export date
2026-08-17
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-17/860dc0eef34653a2a2dab2761771be9cda8410b7a1f078032b37381cbdbb4107/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
Import run
20260818T065550Z
Imported at
2026-08-18 07:28:03
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

For external use only Avoid contact with the eye. Stop and ask a doct if irritation occurs or if there is no improvement within 2 weeks for jock itch or within 4 weeks for athlete's foot & ringworm. Do not use on children under 2 og age except under the advice and supervision of a doctor. Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center right away.