EarWax Removal Kit Rite Aid

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: EarWax Removal Kit Rite Aid
Generic name: CARBAMIDE PEROXIDE 6.5%
Manufacturer: Rite Aid
Product type: HUMAN OTC DRUG
SPL set ID: da78ac58-6c1c-4fa9-baac-e9dec0241385
SPL ID: 0c93ce87-317a-1617-e063-6394a90a618d
Version: 5
Effective date: 2023-12-15
Source export date: 2026-10-30
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/a900515c00f4d0d29f88cc94ee68daf127f036296f87a6b4a8a3f964cd0433c0/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:48:29

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M014	openfda.application_number
brand name		EarWax Removal Kit Rite Aid	openfda.brand_name
generic name		CARBAMIDE PEROXIDE 6.5%	openfda.generic_name
manufacturer name		Rite Aid	openfda.manufacturer_name
ndc	package	11822-1222-7	openfda.package_ndc
ndc	package	11822-1224-1	openfda.package_ndc
ndc	product	11822-1222	openfda.product_ndc
ndc11	package	11822122401	derived:openfda.package_ndc
ndc11	package	11822122207	derived:openfda.package_ndc
rxcui		702050	openfda.rxcui
spl id		0c93ce87-317a-1617-e063-6394a90a618d	id
spl set id		da78ac58-6c1c-4fa9-baac-e9dec0241385	set_id

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 Ask doctor before use if you have • ear drainage or discharge • ear pain • irritation or rash in ear • dizziness • an injury or perforation (hole) of the eardrum • recently had ear surgery When using this product avoid contact with eyes Stop use and ask a doctor if you need to use for more than four days • excessive earwax remains after use of this product Keep out of reach of the children If product is 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.