GoodSense Ear Wax Removal Kit

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 Ear Wax Removal Kit
Generic name: CARBAMIDE PEROXIDE
Manufacturer: Geiss, Destin & Dunn, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 31ea324f-a9a1-7865-e063-6294a90a92e8
SPL ID: 3f2f88ef-2715-ebff-e063-6394a90ae84a
Version: 2
Effective date: 2025-09-19
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:46:05

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M014	openfda.application_number
brand name		GoodSense Ear Wax Removal Kit	openfda.brand_name
generic name		CARBAMIDE PEROXIDE	openfda.generic_name
manufacturer name		Geiss, Destin & Dunn, Inc	openfda.manufacturer_name
ndc	package	50804-117-01	openfda.package_ndc
ndc	package	50804-117-11	openfda.package_ndc
ndc	product	50804-117	openfda.product_ndc
ndc11	package	50804011701	derived:openfda.package_ndc
ndc11	package	50804011711	derived:openfda.package_ndc
rxcui		702050	openfda.rxcui
spl id		3f2f88ef-2715-ebff-e063-6394a90ae84a	id
spl set id		31ea324f-a9a1-7865-e063-6294a90a92e8	set_id
unii		31PZ2VAU81	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

Do not use if you have ear drainage or discharge, ear pain, irritation or rash in the ear or are dizzy; consult a doctor if you have an injury or perforation (hole) in the ear drum or after ear surgery, unless directed by a doctor for more than 4 days; if excessive earwax remains after use of this product, consult a doctor When using this product avoid contact with yes. If accidental contact with yes occurs, flush eyes with water and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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