FDA label f1c95a60-2b74-e875-e053-2a95a90ac9f4

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
af88af65-c519-1f20-e053-2a95a90a195f
SPL ID
f1c95a60-2b74-e875-e053-2a95a90ac9f4
Version
2
Effective date
2023-01-08
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:58:14

Warnings cross-check#

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

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only Flammable Keep away from fire or flame, heat, spark, electrical. Flash point 72°F. do not use with eletocautery procedures. Ask a doctor before use if you have deep or puncture 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 1 week unless directed by a doctor Stop use and ask a doctor if condition persists or gets worse

warnings and cautions

Other information does not contain, nor is intended as a substitue for grain or ethyl alcohol. will produce serious gastric disturbances if taken internally.

Reported adverse events (FAERS/openFDA)#

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