FDA label 873a0104-934c-45e8-849b-693d837da853

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
848cfd76-aa0a-427b-959f-66d2cf5f9a34
SPL ID
873a0104-934c-45e8-849b-693d837da853
Version
2
Effective date
2017-12-07
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:25:34

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

Warning: For external use only When using this product • avoid contact with eyes and nose • do not apply to large areas of the body • do not put into rectum using fingers, mechanical device or applicator Stop use and ask a doctor If: • condition worsens • symptoms persist for more than 7 days or recur again within a few days • you develop allergic reaction, redness, irritation, swelling or pain • rectal bleeding occurs

Reported adverse events (FAERS/openFDA)#

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