PREPARATION H FOR WOMEN

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: PREPARATION H FOR WOMEN
Generic name: WITCH HAZEL
Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
SPL set ID: a9099cf4-4e2e-4cf1-a52f-48f8e174cb15
SPL ID: 47e7adb3-c8ce-b0b9-e063-6394a90a7e0c
Version: 10
Effective date: 2026-01-08
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 05:18:55

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		PREPARATION H FOR WOMEN	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Haleon US Holdings LLC	openfda.manufacturer_name
ndc	package	0573-0559-41	openfda.package_ndc
ndc	package	0573-0559-10	openfda.package_ndc
ndc	package	0573-0559-40	openfda.package_ndc
ndc	product	0573-0559	openfda.product_ndc
ndc11	package	00573055940	derived:openfda.package_ndc
ndc11	package	00573055941	derived:openfda.package_ndc
ndc11	package	00573055910	derived:openfda.package_ndc
rxcui		1544863	openfda.rxcui
spl id		47e7adb3-c8ce-b0b9-e063-6394a90a7e0c	id
spl set id		a9099cf4-4e2e-4cf1-a52f-48f8e174cb15	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 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 reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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