Timolol Maleate Solution/ Drops
Product Images NDC 60758-801

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Timolol Maleate (NDC 60758-801). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pacific 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

Timolol Solution 01

Timolol Solution 01
A text excerpt presenting optical rotation data for timolol maleate in 1.0N hydrochloric acid (5% concentration), listing a specific rotation value measured at 405 nm wavelength.*
FDA Label Image

Timolol Solution 02

Timolol Solution 02
Chemical structure diagram of the active ingredient timolol maleate shown with labeled atoms and bonds depicting its molecular composition.*
FDA Label Image

Timolol Solution 03

Timolol Solution 03
A data table listing National Drug Codes (NDC) for TIMOLOL MALEATE ophthalmic solution/drops at 2.5 mg/mL and 5 mg/mL strengths. It shows packaging sizes of 5 mL in a 10 mL bottle (NDC 60758-802-05) and 10 mL in a 15 mL bottle (NDC 60758-802-10), labeled by Pacific Pharma, Inc.*
FDA Label Image

Timolol Solution 04

Timolol Solution 04
A data table listing National Drug Codes (NDC) for TIMOLOL MALEATE ophthalmic solution in various bottle sizes. It includes NDC 60758-801-05 for a 5 mL fill in a 10 mL bottle, NDC 60758-801-10 for a 10 mL fill in a 15 mL bottle, and NDC 60758-801-15 for a 15 mL fill in a 15 mL bottle.*
FDA Label Image

Timolol Solution 05

Timolol Solution 05
An instructional black-and-white illustration showing a hand holding an ophthalmic drop bottle tilted downward with the other hand poised to squeeze and dispense drops into the eye. The image demonstrates proper technique for administering timolol maleate ophthalmic solution drops.*
FDA Label Image

Timolol Solution 06

Timolol Solution 06
An instructional illustration showing a hand holding a bottle labeled TIMOLOL MALEATE Ophthalmic Solution, with another hand preparing to instill drops by tilting the bottle and positioning it near an eye. This diagram demonstrates the proper technique for administering timolol maleate ophthalmic solution as eye drops.*
FDA Label Image

Timolol Solution 07

Timolol Solution 07
An instructional illustration showing a close-up side profile of a person administering eye drops into their eye, demonstrating proper ophthalmic drop instillation technique.*
FDA Label Image

Timolol Solution 08

Timolol Solution 08
An instructional black-and-white line drawing depicting an eye receiving ophthalmic drops. The image shows an eye with a drop falling toward it, illustrating the application of eye drops.*
FDA Label Image

Timolol Solution 09

Timolol Solution 09
An instructional illustration showing an eye with a bottle of ophthalmic solution positioned above it, demonstrating the proper method to apply eye drops by placing a drop into the eye.*
FDA Label Image

Timolol Solution 0a

FDA Label Image

Timolol Solution 0b

Timolol Solution 0b
The label for Timolol Maleate Ophthalmic Solution USP 0.25% (timolol equivalent 3.4 mg/mL) in a 10 mL bottle is shown. It is manufactured by Pacific Pharma, Inc. The label includes usage instructions, storage conditions, and a barcode. The product is sterile and designated for prescription use only.*
FDA Label Image

Timolol Solution 0c

Timolol Solution 0c
Packaging label for TIMOLOL MALEATE 0.5% ophthalmic solution, a sterile eye drop solution in a 10 mL bottle by Pacific Pharma, Inc. The label shows timolol maleate equivalent 6.8 mg/mL, Rx only, with dosing, storage instructions, and preservative details included on side panels.*

* 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.