Ear Wax Removal Drops

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: Ear Wax Removal Drops
Generic name: CARBAMIDE PEROXIDE - 6.5%
Manufacturer: GeriCare Pharmaceutical Corp
Product type: HUMAN OTC DRUG
SPL set ID: 239702af-cf93-43ee-b1af-8e53642395c1
SPL ID: 4589c7e6-c807-5a69-e063-6394a90a8b89
Version: 3
Effective date: 2025-12-09
Source export date: 2026-10-12
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:38:32

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		Ear Wax Removal Drops	openfda.brand_name
generic name		CARBAMIDE PEROXIDE - 6.5%	openfda.generic_name
manufacturer name		GeriCare Pharmaceutical Corp	openfda.manufacturer_name
ndc	package	57896-339-05	openfda.package_ndc
ndc	product	57896-339	openfda.product_ndc
ndc11	package	57896033905	derived:openfda.package_ndc
rxcui		702050	openfda.rxcui
spl id		4589c7e6-c807-5a69-e063-6394a90a8b89	id
spl set id		239702af-cf93-43ee-b1af-8e53642395c1	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 Do not use if you are dizzy if you have ear drainage or discharge, ear pain, irritation or rashin the ear. Consult your doctor. if you have an injury or perforation (hole) of the ear drum or after ear surgery, unless directed by a doctor

Reported adverse events (FAERS/openFDA)#

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