ERO 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: ERO Ear Wax Removal Kit
Generic name: CARBAMIDE PEROXIDE 6.5%
Manufacturer: Randob Labs
Product type: HUMAN OTC DRUG
SPL set ID: fbf8a6f2-531d-5047-e053-6294a90aaa01
SPL ID: 29575528-5bed-065e-e063-6394a90a4eca
Version: 2
Effective date: 2024-12-15
Source export date: 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:44

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		ERO Ear Wax Removal Kit	openfda.brand_name
generic name		CARBAMIDE PEROXIDE 6.5%	openfda.generic_name
manufacturer name		Randob Labs	openfda.manufacturer_name
ndc	package	52412-175-01	openfda.package_ndc
ndc	product	52412-175	openfda.product_ndc
ndc11	package	52412017501	derived:openfda.package_ndc
rxcui		702050	openfda.rxcui
spl id		29575528-5bed-065e-e063-6394a90a4eca	id
spl set id		fbf8a6f2-531d-5047-e053-6294a90aaa01	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

Ask a doctor before use if you have if you have ear drainage or discharge, ear pain, irritation or rash in the ear, dizziness an injury or perforation (hole) of the eardrum, 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 four days, excessive earwax remains after use of this product.

Reported adverse events (FAERS/openFDA)#

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