FDA.reportPublic FDA data

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
2026-08-01
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/2026-08-01/206e0852f7011b53c21719ec5c68ac6752381d0fcd1d348f7428adad64429e89/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:18:11
Harmonized routes table
Harmonized routes
TOPICAL

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.