GOODSENSE Maximum Strength Medicated

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: GOODSENSE Maximum Strength Medicated
Generic name: WITCH HAZEL
Manufacturer: GEISS, DESTIN & DUNN, INC
Product type: HUMAN OTC DRUG
SPL set ID: 5453a12b-e775-4101-bd3a-337857e9e167
SPL ID: 453a56d2-cd45-a854-e063-6394a90a969d
Version: 6
Effective date: 2025-12-05
Source export date: 2026-10-27
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/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:52:49

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		GOODSENSE Maximum Strength Medicated	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		GEISS, DESTIN & DUNN, INC	openfda.manufacturer_name
ndc	package	50804-211-48	openfda.package_ndc
ndc	product	50804-211	openfda.product_ndc
ndc11	package	50804021148	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		453a56d2-cd45-a854-e063-6394a90a969d	id
spl set id		5453a12b-e775-4101-bd3a-337857e9e167	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.(1-800-222-1222)

Reported adverse events (FAERS/openFDA)#

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