FDA.reportPublic FDA data

FDA label b5aa571c-c045-4bd4-e053-2995a90a6acb

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
b5aa5700-977e-7f3f-e053-2a95a90a82eb
SPL ID
b5aa571c-c045-4bd4-e053-2995a90a6acb
Version
1
Effective date
2020-12-04
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 07:58:22

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

For external use only Do not use on areas with wounds, eczema, or dermatitis. Stop use and ask a doctor if you have a. Redness, swelling, itchiness, irritation, or other similar symptoms. b. Occurrence of the above symptoms upon exposure to direct sunlight. When using this product, keep out of eyes. If eye contact occurs, rinse well with water. Keep out of reach of children. If product is 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.