Maximum Strength 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: Maximum Strength Hemorrhoidal Pads
Generic name: WITCH HAZEL
Manufacturer: Walmart, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 6dd8d3d9-5109-4869-917b-9521e9ba1ed0
SPL ID: 39e9aa87-d355-96dc-e063-6294a90a1c4b
Version: 3
Effective date: 2025-07-14
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:20:36

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Maximum Strength Hemorrhoidal Pads	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Walmart, Inc.	openfda.manufacturer_name
ndc	package	49035-465-10	openfda.package_ndc
ndc	package	49035-465-20	openfda.package_ndc
ndc	product	49035-465	openfda.product_ndc
ndc11	package	49035046520	derived:openfda.package_ndc
ndc11	package	49035046510	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		39e9aa87-d355-96dc-e063-6294a90a1c4b	id
spl set id		6dd8d3d9-5109-4869-917b-9521e9ba1ed0	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 exceed the recommended daily dosage unless directed by a doctor do not insert into rectum or vagina using fingers or any 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 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.