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
Medical Products Laboratories, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
b815792f-2f8f-7ac8-e053-2995a90ade18
SPL ID
28dabfcb-f8d9-6b91-e063-6394a90a800c
Version
3
Effective date
2024-12-11
Source export date
2026-11-06
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/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:46:38
Harmonized routes table
Harmonized routes
TOPICAL

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 last for more than 7 days Keep out of reach of children. If swallowed, get medical help or contact a Posion Control Center right away. MANUFACTURED BY: MEDICAL PRODUCTS LABORATORIES, INC. 9990 GLOBAL ROAD, PHILADELPHIA 19115 mplusa.com Questions or comments? Call 1-800-523-0191

Reported adverse events (FAERS/openFDA)#

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