FDA.reportPublic FDA data

FDA label e9c06ce6-ecd6-951c-e053-2995a90afb60

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
4edb57ea-e947-42e7-8d6c-ff83388aed7c
SPL ID
e9c06ce6-ecd6-951c-e053-2995a90afb60
Version
6
Effective date
2022-09-28
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:02:50

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 use in or near the eyes do not exceed recommended daily dosage unless directed by a doctor do not put this product in to the rectum by using fingers or any mechanical device Stop use and ask a doctor if condition worsens or does not improve within 7 days. In case of bleeding, consult a doctor promptly. 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.