FDA label e7507fd7-8026-4327-a52b-8aa13b2e20a3

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
220bf5c6-b113-46fa-924d-8093473e2a30
SPL ID
e7507fd7-8026-4327-a52b-8aa13b2e20a3
Version
2
Effective date
2015-11-12
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:04:26

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 When using this product Avoid contact with the eyes Do not put in rectum Do not exceed recommended dosage unless directed by a doctor Stop use and ask a doctor if allergic reaction occurs condition worsens or does not improve within 7 days Symptoms clear up and return within a few days rectal bleading occurs redness irritation swelling pain or other symptoms develop or increase

Reported adverse events (FAERS/openFDA)#

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