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: TOP CARE (Topco Associates LLC)
Product type: HUMAN OTC DRUG
SPL set ID: 23b592f7-3af3-45ef-897a-fe33ab518b6d
SPL ID: 3b664a3e-029c-44e7-9592-679fe5099b1c
Version: 8
Effective date: 2025-04-14
Source export date: 2026-11-06
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:00:45

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 · 10 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		TOP CARE (Topco Associates LLC)	openfda.manufacturer_name
ndc	package	36800-039-16	openfda.package_ndc
ndc	product	36800-039	openfda.product_ndc
ndc11	package	36800003916	derived:openfda.package_ndc
spl id		3b664a3e-029c-44e7-9592-679fe5099b1c	id
spl set id		23b592f7-3af3-45ef-897a-fe33ab518b6d	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 avoid swallowing 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 persist for more than 7 days. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away..

Reported adverse events (FAERS/openFDA)#

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