PREPARATION H MEDICATED 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 MEDICATED WIPES
Generic name: WITCH HAZEL
Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
SPL set ID: 8d9961f0-1ecf-d7fb-b6b4-856d636d68e1
SPL ID: 4d3a65fc-cb79-5f92-e063-6294a90ad3c3
Version: 12
Effective date: 2026-03-17
Source export date: 2026-10-27
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/2c7d3f7bcea1543046130e07dcbaf7eea5fb0ce23f7faa6458d1c6d80c3fa0c3/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:42:06

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		PREPARATION H MEDICATED WIPES	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Haleon US Holdings LLC	openfda.manufacturer_name
ndc	package	0573-0556-98	openfda.package_ndc
ndc	package	0573-0556-95	openfda.package_ndc
ndc	package	0573-0556-07	openfda.package_ndc
ndc	package	0573-0556-20	openfda.package_ndc
ndc	package	0573-0556-96	openfda.package_ndc
ndc	product	0573-0556	openfda.product_ndc
ndc11	package	00573055695	derived:openfda.package_ndc
ndc11	package	00573055696	derived:openfda.package_ndc
ndc11	package	00573055607	derived:openfda.package_ndc
ndc11	package	00573055620	derived:openfda.package_ndc
ndc11	package	00573055698	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		4d3a65fc-cb79-5f92-e063-6294a90ad3c3	id
spl set id		8d9961f0-1ecf-d7fb-b6b4-856d636d68e1	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.