FDA label 25cfb264-0ff0-49b8-881a-8c2a40e4134d

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
f72e9a3c-a194-4b71-961f-f811b22185e9
SPL ID
25cfb264-0ff0-49b8-881a-8c2a40e4134d
Version
1
Effective date
2017-10-10
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 03:04:37

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 do not get into eyes. Stop use and ask a doctor if • condition worsens or does not improve within 7 days • do not exceed the recommended daily dosage unless directed by a doctor • in case of bleeding, consult a doctor promptly • do not put this product into the rectum by using fingers or any mechanical device or applicator certan persons can develop allergic reactions to ingredients in this product. If the simptoms being treated does not subside or if redness, irritation, swelling, or other simproms develop or increase, discontinue use and consult a doctor Keep out of reach of children. If 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.