FDA label 42c804c8-dcab-4f72-8b93-be5728602a18

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
af0c4fef-6fcb-41b5-a0a6-70d9b7f625a5
SPL ID
42c804c8-dcab-4f72-8b93-be5728602a18
Version
2
Effective date
2011-02-16
Source export date
2026-11-06
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:20:04

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. _______________________________ Do not use on: - puncture wounds or deep wounds - animal bites - serious burns _______________________________ Keep product away from eyes. _______________________________ Stop use and ask a doctor if: -condition worsens -symptoms last more than 7 days; clear up and occur again within several days

Reported adverse events (FAERS/openFDA)#

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