FDA label 2e5dcbca-97ab-4257-a084-9ee85b41d874

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
4e2a0942-0d17-4698-a6f7-9afe0b75cf2d
SPL ID
2e5dcbca-97ab-4257-a084-9ee85b41d874
Version
3
Effective date
2012-05-23
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 06:02:00

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. Allergy alert: Do not use if allergic to any ingredients. Do not use in the eyes over large areas of the body Ask a doctor before use if you have Deep or puncture wounds Animal bites Serious burns Stop use and ask doctor if You need to use longer than 1 week Condition persists or gets worse Symptoms persist for more than 1 week, or clear up and occur again within a few days Rash or other allergic reaction develops

Reported adverse events (FAERS/openFDA)#

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