FDA.reportPublic FDA data

FDA label f3b1d701-169b-b3a2-e053-2a95a90ae9f5

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
06dbbb55-9464-4c50-9fb1-cc1c4496c60a
SPL ID
f3b1d701-169b-b3a2-e053-2a95a90ae9f5
Version
5
Effective date
2023-02-02
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:12:46

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 in the eyes if you are allergic to any of the ingredients over large areas of the body • ASK A DOCTOR BEFORE USE IF YOU HAVE Animal bites Serious burns Deep or puncture wounds • STOP USE AND ASK A DOCTOR IF You need to use longer than 1 week Condition persists or gets worse Rash or other allergic reaction develops • 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.