Medicated 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: Medicated Hemorrhoidal Pads
Generic name: WITCH HAZEL
Manufacturer: Cardinal Health
Product type: HUMAN OTC DRUG
SPL set ID: 0b49db40-7abc-4e62-b6da-4b9f5b0ae16d
SPL ID: 4539d93f-d5be-fdbe-e063-6294a90a8c51
Version: 8
Effective date: 2025-12-05
Source export date: 2026-10-27
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:57:51

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		M016	openfda.application_number
brand name		Medicated Hemorrhoidal Pads	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Cardinal Health	openfda.manufacturer_name
ndc	package	70000-0364-1	openfda.package_ndc
ndc	product	70000-0364	openfda.product_ndc
ndc11	package	70000036401	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		4539d93f-d5be-fdbe-e063-6294a90a8c51	id
spl set id		0b49db40-7abc-4e62-b6da-4b9f5b0ae16d	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 use only. When using this product do not use more than directed unless told to do so by a doctor do not put directly in the rectum by using fingers or any mechanical device or applicator. Stop use and ask a doctor if bleeding occurs condition worsens or does not improve within 7 days Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away. (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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