Swim-ear Solution
Product Images NDC 0168-0126

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 Swim-ear (NDC 0168-0126). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fougera Pharmaceuticals, Llc, 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

Package Label – Principal Display Panel – 1/2 Oz Container (Swimear1)

Package Label – Principal Display Panel – 1/2 Oz Container (Swimear1)
Swim-EAR ear drying aid solution, 950 mg/mL, in a 29.57 mL (1 fl oz) bottle by Fougera Pharmaceuticals, LLC. The label shows the product name with a graphic of a diver, an NDC code 0168-0126-91, active ingredient isopropyl alcohol 95%, usage directions for drying ears, warnings including flammability and safety precautions, and inactive ingredient anhydrous glycerin 5% base.*
FDA Label Image

Package Label – Principal Display Panel – 1/32 Oz Container (Swimear2)

Package Label – Principal Display Panel – 1/32 Oz Container (Swimear2)
Packaging label for Swim-EAR 950 mg/mL solution, an ear drying aid by Fougera Pharmaceuticals, LLC. The front highlights the product name Swim-EAR with a bottle image and states it dries water in the ears and relieves water-clogged ears. The label indicates a 29.57 mL (1 fl oz) bottle size and emphasizes the product's use for ear drying. The side panels include drug facts listing isopropyl alcohol 95% as the active ingredient and anhydrous glycerin 5% as inactive ingredient, along with uses, warnings, directions, and manufacturer information.*

* 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.