FDA label 784ef895-d19f-4ab2-a26e-8eab661e4b02

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
96af69b6-42ed-4327-8fa5-a64dfc19d2ec
SPL ID
784ef895-d19f-4ab2-a26e-8eab661e4b02
Version
2
Effective date
2013-05-10
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:28:48

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. Keep out of reach of children. If ingested, get medical help or contact a Poison Control Center right away. Do not use in eyes in large quantities over raw or blistered areas, or on deep puncture wounds, animal bites, serious burns for more than one week unless directed by a doctor Stop use and ask a doctor if the condition gets worse condition clears up and recurs within a few days condition persists for more than 7 days

Reported adverse events (FAERS/openFDA)#

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