Meijer Earwax 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: Meijer Earwax Removal Kit
Generic name: CARBAMIDE PEROXIDE
Manufacturer: Meijer Distribution Inc.
Product type: HUMAN OTC DRUG
SPL set ID: a5f7bd55-55c3-4b0e-a16c-33bbea40536a
SPL ID: 52f6676c-1f3c-0643-e063-6294a90a7995
Version: 5
Effective date: 2026-05-29
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:39:47

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		M014	openfda.application_number
brand name		Meijer Earwax Removal Kit	openfda.brand_name
generic name		CARBAMIDE PEROXIDE	openfda.generic_name
manufacturer name		Meijer Distribution Inc.	openfda.manufacturer_name
ndc	package	41250-835-33	openfda.package_ndc
ndc	product	41250-835	openfda.product_ndc
ndc11	package	41250083533	derived:openfda.package_ndc
rxcui		702050	openfda.rxcui
spl id		52f6676c-1f3c-0643-e063-6294a90a7995	id
spl set id		a5f7bd55-55c3-4b0e-a16c-33bbea40536a	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

Warnings For use in the ear only Ask a doctor before use if you have • ear drainage or discharge • ear pain • irritation, or rash in the ear • dizziness • an injury or perforation (hole) of the ear drum • recently had ear surgery When using this product avoid contact with the eyes Stop use and ask a doctor if • you need to use for more than 4 days • excessive earwax remains after use of this product 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.