FDA label 2c63eb8e-f6bd-4278-b5bc-e461ded213fd

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
09fd53f4-bc5b-4b0b-a838-cb6d56effc71
SPL ID
2c63eb8e-f6bd-4278-b5bc-e461ded213fd
Version
21
Effective date
2021-08-19
Source export date
2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:48:44

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 •animal bites •serious burns When using this product •do not get into eyes Stop use and ask a doctor if •condition worsens •symptoms last more tan 7 days or clear up and occur again within a few days •if redness, irritation, or swelling or pain persists or increases Keep out of reach of children. If swallowed, get medical help or contact a Poison control Center right away.

Reported adverse events (FAERS/openFDA)#

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