hemorrhoidal pads

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: hemorrhoidal pads
Generic name: WITCH HAZEL
Manufacturer: Meijer Distribution Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 53e39d22-a89e-4f95-8c64-abeb50f72ce7
SPL ID: 39ad74f5-b6ff-96bf-e063-6394a90a3585
Version: 4
Effective date: 2025-07-11
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 06:04:51

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		hemorrhoidal pads	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Meijer Distribution Inc.	openfda.manufacturer_name
ndc	package	41250-868-10	openfda.package_ndc
ndc	product	41250-868	openfda.product_ndc
ndc11	package	41250086810	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		39ad74f5-b6ff-96bf-e063-6394a90a3585	id
spl set id		53e39d22-a89e-4f95-8c64-abeb50f72ce7	set_id
unii		101I4J0U34	openfda.unii

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 rectal use only. When using this product do not exceed the recommended daily dosage unless directed by a doctor. do not insert into rectum or vagina using fingers or mechanical device. Stop use and ask a doctor if rectal bleeding occurs condition worsens or does not improve within 7 days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Reported adverse events (FAERS/openFDA)#

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