Witch Hazel

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: Witch Hazel
Generic name: MEDICATED HEMORRHOIDAL WIPES
Manufacturer: Giant Eagle
Product type: HUMAN OTC DRUG
SPL set ID: cdd9d6b7-cbc9-2839-e053-2a95a90ada00
SPL ID: 453a4e53-3ebc-9d68-e063-6294a90a3125
Version: 4
Effective date: 2025-12-05
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:34:39

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		Witch Hazel	openfda.brand_name
generic name		MEDICATED HEMORRHOIDAL WIPES	openfda.generic_name
manufacturer name		Giant Eagle	openfda.manufacturer_name
ndc	package	56194-550-01	openfda.package_ndc
ndc	product	56194-550	openfda.product_ndc
ndc11	package	56194055001	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		453a4e53-3ebc-9d68-e063-6294a90a3125	id
spl set id		cdd9d6b7-cbc9-2839-e053-2a95a90ada00	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 recommendeed daily dosage unless directed by a doctor. Do not put this product into 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 the 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.