PREPARATION H SOOTHING RELIEF CLEANSING AND COOLING WIPES

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 SOOTHING RELIEF CLEANSING AND COOLING WIPES
Generic name: WITCH HAZEL
Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
SPL set ID: 485437a8-b2e9-4acf-a20e-edb1f08a9cae
SPL ID: 5190224a-ec77-c801-e063-6294a90a80d8
Version: 5
Effective date: 2026-05-11
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 06:06:32

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		PREPARATION H SOOTHING RELIEF CLEANSING AND COOLING WIPES	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Haleon US Holdings LLC	openfda.manufacturer_name
ndc	package	0573-0553-60	openfda.package_ndc
ndc	package	0573-0553-95	openfda.package_ndc
ndc	product	0573-0553	openfda.product_ndc
ndc11	package	00573055360	derived:openfda.package_ndc
ndc11	package	00573055395	derived:openfda.package_ndc
rxcui		1544863	openfda.rxcui
spl id		5190224a-ec77-c801-e063-6294a90a80d8	id
spl set id		485437a8-b2e9-4acf-a20e-edb1f08a9cae	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.