Good Sense 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: Good Sense Medicated
Generic name: WITCH HAZEL
Manufacturer: Geiss, Destin & Dunn, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 5f122db5-4391-4957-9c25-76834c356c4f
SPL ID: 453a4c7b-fc29-b5cf-e063-6394a90addbf
Version: 6
Effective date: 2025-12-05
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:12:40

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		Good Sense Medicated	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Geiss, Destin & Dunn, Inc	openfda.manufacturer_name
ndc	package	50804-047-60	openfda.package_ndc
ndc	product	50804-047	openfda.product_ndc
ndc11	package	50804004760	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		453a4c7b-fc29-b5cf-e063-6394a90addbf	id
spl set id		5f122db5-4391-4957-9c25-76834c356c4f	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 contact with eyes. Stop use and ask a doctor if condition worsens or does not improve within 7 days in case of bleeding Do Not Use Do not put this product into rectum using fingers or any mechanical device or applicator Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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