FDA label 299550cd-e0af-3ad3-e063-6294a90a460e

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)

SPL set ID
09e28a7d-9b89-4b97-bfab-111bdc025299
SPL ID
299550cd-e0af-3ad3-e063-6294a90a460e
Version
5
Effective date
2024-12-18
Source export date
2026-09-28
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:41:30

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 on irritated skin, infected or reddened areas, moles, birthmarks, warts with hair growing from them, genital warts, warts on the face or mucous membrane. diabetes or poor blood circulation. Avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes. Stop use and ask a doctor if discomfort persists. Cap tube tightly and store at room temperature away from heat. For external use only. Do not use Ask a doctor before use if you have Avoid inhaling vapors. Flammable. Keep away from fire and flame. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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