FDA.reportPublic FDA data

FDA label a1178cf3-1b92-1dc7-e053-2a95a90a578b

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
73a574df-2c74-3609-e053-2991aa0a895d
SPL ID
a1178cf3-1b92-1dc7-e053-2a95a90a578b
Version
2
Effective date
2020-03-17
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:32:14

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.