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: WITCH HAZEL
Manufacturer: Topco Associates LLC
Product type: HUMAN OTC DRUG
SPL set ID: 471a9f8d-ba12-41d3-a510-20c1a13ff850
SPL ID: 4ab9bfe0-d6b8-9473-e063-6294a90ad884
Version: 9
Effective date: 2026-02-13
Source export date: 2026-11-06
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/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:55:37

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		WITCH HAZEL	openfda.generic_name
manufacturer name		Topco Associates LLC	openfda.manufacturer_name
ndc	package	76162-822-43	openfda.package_ndc
ndc	product	76162-822	openfda.product_ndc
ndc11	package	76162082243	derived:openfda.package_ndc
rxcui		200295	openfda.rxcui
spl id		4ab9bfe0-d6b8-9473-e063-6294a90ad884	id
spl set id		471a9f8d-ba12-41d3-a510-20c1a13ff850	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 avoid contact with the eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if condition worsens or symptoms persists for more than 7 days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTION DISTRIBUTED BY TOPCO ASSOCIATES LLC ELK GROVE VILLAGE, IL 60007 TOPCO VIJA0718 Questions? 1-888-423-0139 topcare @topco.com www.topcarebrand.com QUALITY GUARANTEED Pat. D675, 101

Reported adverse events (FAERS/openFDA)#

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