Neilmed Clear Canal Earwax Removal Kit Solution/ Drops
Product Images NDC 13709-314

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Neilmed Clear Canal Earwax Removal Kit (NDC 13709-314). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Neilmed Pharmaceuticals Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Neilmed Clearcanal Earwax Removal Kit (2729 Enu Us Rev1 Page 0001)

Neilmed Clearcanal Earwax Removal Kit (2729 Enu Us Rev1 Page 0001)
NeilMed Clear Canal Earwax Removal Complete Kit packaging label features the product name prominently along with Dr. Mehta's branding. The label highlights the solution strength as carbamide peroxide 65 mg/mL (earwax softener), designed for auricular use. The kit contains a saline spray bottle, soft ear plugs, a drainage collection cup, and a waxout tool, totaling five complete treatments. Manufactured by NeilMed Pharmaceuticals Inc, the packaging includes directions, warnings, drug facts, and usage instructions.*
FDA Label Image

Clearcanal Earwax Removal Saline Spray (4081 Enu Us Rev2 Page 0001)

Clearcanal Earwax Removal Saline Spray (4081 Enu Us Rev2 Page 0001)
Label for NeilMed Clear Canal Earwax Removal Saline Spray with Carbamide Peroxide 65 mg/mL solution. The label highlights pH balanced, buffered saline solution in a 2.7 oz (75.2 g) isotonic saline bottle. It includes warnings, ingredients, directions for spray use, manufacturer NeilMed Pharmaceuticals Inc, address, and storage instructions on a purple background.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.