Ear Wax Removal Aid 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 Aid Drops
Generic name: CARBAMIDE PEROXIDE
Manufacturer: PHARMACY VALUE ALLIANCE, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 85ae80c1-2bc2-4c90-9559-63510d03e739
SPL ID: bbd28093-02a5-4201-abf5-13670eac97e4
Version: 6
Effective date: 2024-10-28
Source export date: 2026-10-12
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:28:56

Harmonized routes table
Harmonized routes
AURICULAR (OTIC)

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		M022	openfda.application_number
brand name		Ear Wax Removal Aid Drops	openfda.brand_name
generic name		CARBAMIDE PEROXIDE	openfda.generic_name
manufacturer name		PHARMACY VALUE ALLIANCE, LLC	openfda.manufacturer_name
ndc	package	68016-793-15	openfda.package_ndc
ndc	product	68016-793	openfda.product_ndc
ndc11	package	68016079315	derived:openfda.package_ndc
rxcui		702050	openfda.rxcui
spl id		bbd28093-02a5-4201-abf5-13670eac97e4	id
spl set id		85ae80c1-2bc2-4c90-9559-63510d03e739	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 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 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 ear wax remains after use this product Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away at (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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