Sunshine HemorrhoidRelief

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
Sunshine HemorrhoidRelief
Generic name
HEMORRHOID SUPPOSITORY
Manufacturer
Apcco Labs, Inc
Product type
HUMAN OTC DRUG
SPL set ID
37de3cb4-f31e-0da7-e063-6294a90a78bf
SPL ID
37de3cb4-f31f-0da7-e063-6294a90a78bf
Version
1
Effective date
2025-06-18
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:15:21
Harmonized routes table
Harmonized routes
RECTAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: For rectal use only. Not for oral consumption. Do not use if you have never had a hemorrhoid diagnosed by a doctor • If you are allergic to any of the ingredients. When using this product, do not exceed the recommended dose. Ask a doctor before use if you have heart disease • high blood pressure • thyroid disease• diabetes • difficulty urinating due to an enlarged prostate gland • bleeding hemorrhoids • a sudden change in bowel habits that persists for 2 weeks Stop use and ask a doctor. If bleeding occurs • If condition worsens or does not improve within 7 days • If redness, irritation, swelling, pain, or other symptoms develop

Reported adverse events (FAERS/openFDA)#

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