FDA label 33ac1ded-838c-1150-e054-00144ff8d46c

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
37893db5-7709-4c89-87c8-10044e41ceaa
SPL ID
33ac1ded-838c-1150-e054-00144ff8d46c
Version
3
Effective date
2016-05-25
Source export date
2026-09-28
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/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:31:51

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. Use as directed. When using this product, do not exceed the recommended daily dosage unless directed by a doctor. Do not insert this product into rectum using fingers or any mechanical device. Keep out of reach of children. Children under 12 should consult physian prior to use. Stop using this product if: Condition worsens or does not improve within seven days. Bleeding occurs. Redness, irritations, swelling, pain or other symptons develop

Reported adverse events (FAERS/openFDA)#

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