Hemorrhoidal Hygiene 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 Hygiene pads
Generic name: WITCH HAZEL
Manufacturer: Akron Pharma Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 936a0cca-5049-4ddf-9581-75c2da6d9cfa
SPL ID: 48386f11-7b80-5bde-e063-6394a90add66
Version: 5
Effective date: 2026-01-12
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:08:44

Harmonized routes table
Harmonized routes
RECTAL

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 Hygiene pads	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Akron Pharma Inc.	openfda.manufacturer_name
ndc	package	71399-0110-1	openfda.package_ndc
ndc	product	71399-0110	openfda.product_ndc
ndc11	package	71399011001	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		48386f11-7b80-5bde-e063-6394a90add66	id
spl set id		936a0cca-5049-4ddf-9581-75c2da6d9cfa	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 Avoid contact with the eyes Consult a doctor If condition worsens or does not improve within 7 days In case of bleeding Before exceeding the recommended dosage DO NOT put this product into the rectum using fingers or any mechanical device.

Reported adverse events (FAERS/openFDA)#

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