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
2026-09-28
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/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:19
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.