FDA label 1831d64a-41a9-9a91-e063-6294a90a1aff

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
16472c5c-7063-4f0a-a86d-3de168d5408d
SPL ID
1831d64a-41a9-9a91-e063-6294a90a1aff
Version
10
Effective date
2024-05-11
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:03:07

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 ONLY DO NOT USE: ON DEEP PUNCTURE WOUNDS ON INFECTIONS ON LACERATIONS WHEN USING THIS PRODUCT: AVOID CONTACT WITH EYES STOP USE AND ASK A DOCTOR IF: CONDITION WORSENS OR DOES NOT IMPROVE WITHIN 7 DAYS

Reported adverse events (FAERS/openFDA)#

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