Ear Wax Removal Drops Solution/ Drops
Product Images NDC 11673-761

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ear Wax Removal Drops (NDC 11673-761). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target Corporation, 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

590878_targetearkit_carton.jpg (590878 Targetearkit Carton)

Packaging label for Ear Wax Removal Drops Up and Up, containing carbamide peroxide 6.5% (65 mg/mL) in a 0.5 FL OZ (15 mL) solution/drops form. The label features product branding with the up & up logo, directions, drug facts, and a bottle image. The labeler is Target Corporation.*

FDA Label Image

590882_eardrops_carton.jpg (590882 Eardrops Carton)

Packaging label for Up and Up Ear Wax Removal Drops containing carbamide peroxide 6.5% solution. The box shows the product name, active ingredient strength (65 mg/mL), and volume (0.5 FL OZ/15 mL). It includes Drug Facts panels with usage, warnings, directions, and inactive ingredients. The labeler is Target Corporation, and the product NDC is 11673-761.*

FDA Label Image

790879_targetearwaxdrops_label.jpg (790879 Targetearwaxdrops Label)

Label for Ear Wax Removal Drops Up and Up, containing carbamide peroxide 6.5% solution/drops. The label features the up & up brand logo and indicates a 0.5 FL OZ (15 mL) bottle. It includes usage instructions, warnings, storage information, and distributor details for Target Corporation, Minneapolis, MN.*

* 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.