Timoptic In Ocudose Solution
Product Images NDC 69918-601

4 FDA label images from Nordic Pharma, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Timoptic In Ocudose (NDC 69918-601). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nordic Pharma, 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

Formula (Image 01)

Formula (Image 01)
Chemical structure diagram of Timolol Maleate, the active ingredient in Timoptic in Ocudose 5 mg/mL ophthalmic solution, showing the molecular arrangement and bonds between atoms.*
FDA Label Image

Label1 (Nordic)

FDA Label Image

Timo Carton .25 (25carton)

Timo Carton .25 (25carton)
Packaging label for Timolol Maleate Ophthalmic Solution, USP 0.5%, a sterile eye drop solution. The product is in 60 single-dose vials of 0.3 mL each. Label states topical use for the eye, preservative-free formulation, and Rx only. Manufactured by Amring Pharmaceuticals Inc. with additional manufacturing by Holopack Verpackungstechnik GmbH, Germany.*
FDA Label Image

Timo Foil .25 (25foil)

Timo Foil .25 (25foil)
Label for Timolol Maleate Ophthalmic Solution, USP 0.5%, preservative-free sterile solution for topical eye application. The product is supplied in 10 single-dose vials of 0.3 mL each. Label includes NDC 69918-601-60 and states it is Rx only. Manufacturer information for Amring Pharmaceuticals Inc. and Holopack Verpackungstechnik GmbH is also shown.*

* 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.