ClearCanal Ear Wax Softerner 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
ClearCanal Ear Wax Softerner Drops
Generic name
CARBAMIDE PEROXIDE
Manufacturer
NeilMed Pharmaceuticals, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
0ef2be5b-cc39-48ae-b5c5-e787464dea08
SPL ID
593c33ae-2b75-5130-e063-6294a90ad883
Version
8
Effective date
2026-08-17
Source export date
2026-10-27
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/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 19:46:08
Harmonized routes table
Harmonized routes
AURICULAR (OTIC)

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: Do not use: If you have had an allergic reaction to carbamide peroxide. 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 four consecutive days When using this product: void contact with the eyes Stop use ad ask a doctor if excessive ear wax remains after use of this product for four consecutive days.

Reported adverse events (FAERS/openFDA)#

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