FDA label 5bb413d0-9e03-4bbc-87ab-0aa2163027ba

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
23f90e34-584d-4069-b832-4b4033bb615c
SPL ID
5bb413d0-9e03-4bbc-87ab-0aa2163027ba
Version
1
Effective date
2021-01-22
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:28:21

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 • For external use only; flammable, keep away from fire or flame, heat, spark, electrical, etc. Ask a doctor before use if you have • Deep punctured wounds, animal bites or serious burns When using this product • Do not get into eyes • Do not apply over large areas of the body • Do not use longer than one week unless directed by a doctor Stop using this product if • Condition persists or gets worse Keep this drug out of the reach of children • In case of an accidental ingestion, seek professional assistance or contact a Poison control center (1-800-222-1222) immediately

Reported adverse events (FAERS/openFDA)#

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