ProCure Hemorrhoidal

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)

Brand name
ProCure Hemorrhoidal
Generic name
MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL
Manufacturer
Twin Med LLC
Product type
HUMAN OTC DRUG
SPL set ID
37a4cc43-0d53-f1bf-e063-6394a90a2dc9
SPL ID
37cdd72a-2001-148c-e063-6394a90af289
Version
2
Effective date
2025-06-15
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:55:53
Harmonized routes table
Harmonized routes
RECTAL, TOPICAL

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 Warnings for external and / or intrarectal use only. Ask doctor before use if you have Ask doctor before use if you have heart disease high blood pressure thyroid disease diabetes difficulty in urination due to enlargement of the prostate gland Ask a doctor or pharmacist before use if you Ask a doctor or pharmacist before use if you are presently taking a prescription drug for high blood pressure or depression When using this product When using this product do not exceed the recommended daily dosage unless directed by a doctor Stop use and ask a doctor if Stop use and ask a doctor if bleeding occurs condition worsens or does not improve within 7 days introduction of applicator into the rectum causes additional pain If pregnant or breast-feeding If pregnant or breast-feeding , ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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