Folliculitis Treatment 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
Folliculitis Treatment Cream
Generic name
MICONAZOLE NITRATE
Manufacturer
TAGRID LLC
Product type
HUMAN OTC DRUG
SPL set ID
32396be0-f74a-5483-e063-6294a90ab3ae
SPL ID
df9c4cbf-0be3-46db-9e66-40c6a2b5f0c1
Version
2
Effective date
2025-04-07
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:26:27
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 Do not use On children under 2 years of age unless directed by a doctor. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. If swallowed,get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if Irritation occurs. There is no improvement within 4 weeks. Discomfort persists. Store at 59-86°F (15-30°C). Close the cap tightly after use. support@tagridllc.com

Reported adverse events (FAERS/openFDA)#

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