ClearCanal Ear Wax Softerner Drops

ClearCanal Ear Wax Softerner Drops is an FDA-registered drug product whose active ingredient is CARBAMIDE PEROXIDE. It is labelled by NeilMed Pharmaceuticals, Inc. taken by auricular (otic) and marketed as a human otc drug product. Identifiers on file: NDC 13709-230, application M014, label effective 20260817. It is one of 18 FDA drug label records sharing the active ingredient CARBAMIDE PEROXIDE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing CARBAMIDE PEROXIDE are most often described in connection with: ear wax, removal drops, years age, directions step, only adults, tilt head, tip applicator, canal keep. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Ear Wax Removal Drops Directions Step 1 Ear Wax Removal Drops Directions: FOR USE IN THE EAR ONLY. Adults and children over 12 years of age: tilt head sideways and place 5 to 10 drops into ear. Tip of applicator should not enter ear canal. Keep drops in ear for several minutes by keeping head tilted or placing enclosed ear plugs in ear. Use twice daily for upto 4 days if needed or as directed by a doctor. Any wax remaining after treatment may be removed by gently flushing the ear with NeilMed ClearCanal rinsing system with special ear rinse adapter. Children under 12 years of age: consult a doctor. Ear Wax Removal Drops Directions Ear Wax Removal Drops Directions

Place 5 to 10 drops of 6.5% carbamide peroxide solution into e

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.

FDA lists 18 drug label records with CARBAMIDE PEROXIDE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is ClearCanal Ear Wax Softerner Drops used for?
Ear Wax Removal Drops Directions Step 1 Ear Wax Removal Drops Directions: FOR USE IN THE EAR ONLY. Adults and children over 12 years of age: tilt head sideways and place 5 to 10 drops into ear. Tip of applicator should not enter ear canal. Keep drops in ear for several minutes by keeping head tilted or placing enclosed ear plugs in ear. Use twice daily for upto 4 days if needed or as directed by …

Who makes ClearCanal Ear Wax Softerner Drops?
NeilMed Pharmaceuticals, Inc. is the labeler of record for ClearCanal Ear Wax Softerner Drops. 18 FDA label records share the active ingredient CARBAMIDE PEROXIDE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does ClearCanal Ear Wax Softerner Drops come in?
administered by auricular (otic). Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is ClearCanal Ear Wax Softerner Drops prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing CARBAMIDE PEROXIDE?
Yes. 18 FDA drug label records list CARBAMIDE PEROXIDE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has ClearCanal Ear Wax Softerner Drops been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.