FDA label 503ef007-a5ac-4abc-90b1-b13bd0a05d08

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
edb70750-bea8-4c0f-9453-f2c38d2f05d9
SPL ID
503ef007-a5ac-4abc-90b1-b13bd0a05d08
Version
1
Effective date
2013-12-16
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:48:05

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. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Do not use without consulting a doctor if the condition appears over a large portion of hte body. If condition worsens, or does not improve after using as directed, consult physician. Do not use for prolonged periods without consulting a docotor.

Reported adverse events (FAERS/openFDA)#

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