Harris Teeter Earwax 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: Harris Teeter Earwax Removal Drops
Generic name: CARBAMIDE PEROXIDE 6.5%
Manufacturer: Harris Teeter LLC
Product type: HUMAN OTC DRUG
SPL set ID: dda4c4bf-425e-4fff-e053-2a95a90a51bc
SPL ID: 2958cebe-650c-ea65-e063-6394a90a3f39
Version: 2
Effective date: 2024-12-15
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:18:07

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		Harris Teeter Earwax Removal Drops	openfda.brand_name
generic name		CARBAMIDE PEROXIDE 6.5%	openfda.generic_name
manufacturer name		Harris Teeter LLC	openfda.manufacturer_name
ndc	package	69256-117-01	openfda.package_ndc
ndc	product	69256-117	openfda.product_ndc
ndc11	package	69256011701	derived:openfda.package_ndc
rxcui		702050	openfda.rxcui
spl id		2958cebe-650c-ea65-e063-6394a90a3f39	id
spl set id		dda4c4bf-425e-4fff-e053-2a95a90a51bc	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

Do not use if you have ear drainage or discharge, ear pain, irritation or rash in the ear, or are dizzy; consult a doctor if you have an injury or perforation (hole) of the eardrum or after ear surgery unless directed by a doctor for more than 4 days; if excessive earwax remains after use of this product, consult a doctor When using this product avoid contact with the eyes. If accidental contact with the eyes occurs, flush your eyes with water and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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