Moxifloxacin Ophthalmic Solution Solution/ Drops
Product Images NDC 70756-638

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Moxifloxacin Ophthalmic Solution (NDC 70756-638). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lifestar Pharma Llc, 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

Structure (22d5cd84 26c0 49b0 Afbf 1e9155749cf6 01)

FDA Label Image

Bottle Label (22d5cd84 26c0 49b0 Afbf 1e9155749cf6 02)

Bottle Label (22d5cd84 26c0 49b0 Afbf 1e9155749cf6 02)
This text provides information about an NDC (National Drug Code) for Moxifloxacin Ophthalmic Solution, which is intended for topical ophthalmic use only. Each mL contains moxifloxacin hydrochloride 5.45 mg, equivalent to moxifloxacin 5 mg. The usual dosage instructions are stated to be read in the enclosed insert. It should be stored at 2°C to 25°C (36°F to 77°F). The product is manufactured by Lifestar Pharma LLC in Mahwah, NJ, USA, and states "Made in India" on the label. The text provides additional details such as an expiration date, the revision date, manufacturing code, and other control numbers that may be related to production.*
FDA Label Image

Bottle Carton (22d5cd84 26c0 49b0 Afbf 1e9155749cf6 03)

Bottle Carton (22d5cd84 26c0 49b0 Afbf 1e9155749cf6 03)
This is a description of a moxifloxacin ophthalmic solution in a 35x34.5 mm unvarnished bottle. The solution is sterile and for topical ophthalmic use only. Each mL contains moxifloxacin hydrochloride and inactives like boric acid and sodium chloride. The usual dosage is one drop in the affected eye three times a day for 7 days. The solution should be stored at 2°C to 25°C and kept out of reach of children. It is manufactured in India for Lifestar Pharma LLC based in Mahwah, NJ, USA. The product is labeled with the NDC code 70756-638-25 and is RX only.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.