Betimol Solution/ Drops
Product Images NDC 82584-002

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Betimol (NDC 82584-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Thea 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

Chemical Structure (Betimol 01)

Chemical Structure (Betimol 01)
Chemical structure diagram of timolol, the active ingredient in BETIMOL ophthalmic solution. The diagram shows the molecular structure with atoms and bonds illustrating the chemical composition of timolol.*
FDA Label Image

Principal Display Panel (5 mL Bottle Carton)

Principal Display Panel (5 mL Bottle Carton)
Packaging label for BETIMOL ophthalmic solution 0.25% (timolol equivalent 2.56 mg/mL) by Thea Pharma Inc. The label indicates a 5 mL bottle for topical eye application, includes storage instructions, and lists inactive ingredients and preservative information. The product is Rx only and manufactured in Switzerland.*
FDA Label Image

Principal Display Panel (5 mL Bottle Carton)

Principal Display Panel (5 mL Bottle Carton)
BETIMOL timolol ophthalmic solution 0.5% 5 mL carton label by Thea Pharma Inc. Features include active ingredient timolol hemihydrate 5.12 mg/mL, sterile solution for topical eye use, and storage instructions. The label shows NDC 82584-002-05 with directions for use, manufacturer details, and preservative 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.