FDA.reportPublic FDA data

FDA label 846c196a-5b4e-08d4-e053-2991aa0a4d85

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
846a49a1-c31e-73b9-e053-2a91aa0a0f95
SPL ID
846c196a-5b4e-08d4-e053-2991aa0a4d85
Version
1
Effective date
2019-03-19
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 07:21:05

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

For external use olny. Flammable ■ Keep away from fire, flame, sparks and heated surfaces. Tight cap firmly Stop use and ask a doctor if ■ Condition worsens or symptoms persist for more than 7days or clear up and occur again within a few days When using this product ■ use olny as direct ■ avoid contact with eyes ■ Do not apply to wounds or damage skin ■ do not bandage tightly If pregnant or breast-feeding, ask a health professional before use keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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