FDA label 52adf0e7-14dd-4833-a166-1a4afff4ff11

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
f6bd40be-6f2c-48b0-8a5c-fc0dc7285d29
SPL ID
52adf0e7-14dd-4833-a166-1a4afff4ff11
Version
2
Effective date
2012-12-20
Source export date
2026-11-06
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:43:33

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. If symptoms persist or worsen, consult a physician. Do not use on open skin or sores. Ask a doctor before use if under 18 years of age. Discontinue use if signs of irritation or rash appear. If pregnant or nursing ask a healthcare professional before use. Keep out of reach of children. If swallowed, seek immediate medical help or contact a Poison Control Center right away. Caution: Avoid contact with the eyes. If product comes in contact with the eyes, flush with warm water.

Reported adverse events (FAERS/openFDA)#

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