Timolol Maleate Solution/ Drops
Product Images NDC 42571-398

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Timolol Maleate (NDC 42571-398). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Micro Labs Limited, 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

Timolol-ampullbl.jpg (Timolol Ampullbl)

Label of Timolol Maleate Ophthalmic Solution USP 0.5%, 0.3 mL dropper bottle. The label indicates the product is preservative-free and Rx only. The label features Micro Labs Limited branding and an artwork code.*

FDA Label Image

Timolol-cartonlbl.jpg (Timolol Cartonlbl)

Packaging label for Timolol Maleate Ophthalmic Solution USP 0.5%, containing 6.8 mg/mL timolol maleate equivalent. The solution is preservative-free, sterile, and intended for topical ophthalmic use. The package contains 60 single-dose vials of 0.3 mL each. Manufactured by Micro Labs Limited and for Micro Labs USA, Inc.*

FDA Label Image

Timolol-pouchlbl.jpg (Timolol Pouchlbl)

Timolol Maleate Ophthalmic Solution USP 0.5% (timolol maleate equivalent to 6.8 mg/mL) in 10 single-dose 0.3 mL vials. Topical eye solution labeled for prescription use only by Micro Labs Limited, manufactured for Micro Labs USA, Inc. The label includes storage and usage instructions along with inactive ingredient details.*

FDA Label Image

Timolol-struc.jpg (Timolol Struc)

A table showing optical rotation data for a substance in 1.0N HCl solution at 5% concentration and 25 degrees Celsius, including specific rotation values ranging from -11.7° to -12.5° and measurement at 405 nm wavelength.*

FDA Label Image

Timolol-structure.jpg (Timolol Structure)

Chemical structure of Timolol Maleate, depicting the molecular components and bonds characteristic of the active pharmaceutical ingredient in the ophthalmic solution form.*

* 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.