FDA.reportPublic FDA data

FDA label 423ac0c9-bb0d-49cd-bde2-46791d00f008

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
108d994b-15d4-4c31-b273-dd74df008810
SPL ID
423ac0c9-bb0d-49cd-bde2-46791d00f008
Version
8
Effective date
2025-07-29
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:19:13

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 deep or puncture wounds animals bites serious burns large areas of the body When using this product do not get into eyes or nose not for prolonged use Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days if 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.