FDA label f225eff5-42ee-466e-bee9-64ea2a963213

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
2b176477-087b-49a3-b2f3-4c1d6327137d
SPL ID
f225eff5-42ee-466e-bee9-64ea2a963213
Version
6
Effective date
2017-12-06
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:22:09

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 Allergy alert: • do not use if allergic to any of the ingredients Do not use •in the eyes •over large areas of the body Ask a doctor before use if you have •deep or puncture wounds •animal bites •serious burns When using this product •do not use longer than 1 week unless directed by a doctor Stop use and ask a doctor if •condition persists or gets worse •symptoms last for more than 7 days or clear up and come back within a few days •a rash or other allergic reaction develops 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.