FDA label 3812fdbc-b730-4e10-83ab-4b83931ba020

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
ab7e51bc-a2ce-4559-b291-211d7bbc1b6a
SPL ID
3812fdbc-b730-4e10-83ab-4b83931ba020
Version
2
Effective date
2023-11-03
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:53:19

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 large quantilies, particularly over raw surfaces or blistered areas. • on deep or puncture wounds, animal biles or serious burns When using this product avoid conlacl with eyes Stop use and ask a doctor if • condilion worsens • symploms last more Ihan 7days or clear up and occur again wilhin afew days

Reported adverse events (FAERS/openFDA)#

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