Timoptic In Ocudose Solution
Product Images NDC 24208-498

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Timoptic In Ocudose (NDC 24208-498). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bausch & Lomb Incorporated, 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

Carton5 (05carton)

Packaging label for Timoptic in Ocudose 0.5% ophthalmic solution (timolol maleate) dispenser by Bausch & Lomb Incorporated. The label shows Timolol Equivalent strength of 6.8 mg/mL and indicates the product contains 60 unit doses of 0.3 mL each. The label highlights use for topical application in the eye and notes preservative-free sterile ophthalmic solution.*

FDA Label Image

Carton25 (25carton)

Packaging label for Timoptic in Ocudose 0.25% (timolol maleate ophthalmic solution) dispenser. The label shows the product concentration as 0.25%, equivalent to timolol maleate 3.4 mg/mL, and indicates 60 unit doses of 0.3 mL each. It includes instructions to discard unused portions immediately after use and states the product is for topical application in the eye. The labeler is Bausch & Lomb Incorporated.*

FDA Label Image

Formula (Image 01)

Chemical structure of Timolol Maleate, the active ingredient in Timoptic in Ocudose ophthalmic solution. The diagram shows the molecular formula with specific chemical groups and bonds characteristic of Timolol Maleate.*

FDA Label Image

Chem Structure (Image 02)

A text panel presenting specific optical rotation data, indicating a measurement of -12.2° at 25°C and 405 nm in 1.0N HCl solution with a 5% concentration. The range of measurement is from -11.7° to -12.5°.*

* 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.