FDA label 50c0de03-0145-10bd-e063-6394a90ad3a4

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
8bef552b-b110-4663-9347-f8dba96c8d53
SPL ID
50c0de03-0145-10bd-e063-6394a90ad3a4
Version
1
Effective date
2026-05-01
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 07:18:26

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 • Broken skin • Deep or puncture wounds • Serious burns When using this product avoid contact with the eyes Keep away from face and mouth to avoid breathing powder. Stop use and ask a doctor : • If the condition worsens • Symptoms persist for more than 7 days or clear up and occur again within a few days. • Redness, irritation, swelling, or pain persists or increases. Keep out of reach of children • If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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