FDA label 8eed9d2b-718e-4ae5-a69d-f35c67f7714b

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
9ef927a1-82c9-4503-bb93-4ca0c413a46b
SPL ID
8eed9d2b-718e-4ae5-a69d-f35c67f7714b
Version
1
Effective date
2017-02-17
Source export date
2026-11-06
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/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:57:57

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 this product in or near the eyes. Rinse with water to remove. Do not use on broken skin or open wounds. Stop Use and ask a Physician if a rash occurs, and worsens or if symptoms persist for more than 7 days. When using this product you may feel a tingling or stinging sensation which should go away in a short time.

Reported adverse events (FAERS/openFDA)#

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