Moxifloxacin Solution/ Drops
Product Images NDC 67296-2129

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Moxifloxacin (NDC 67296-2129). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Molecular Structure (F3245022 7db4 463a A87c 550b4dc40201 01)

Chemical structure of moxifloxacin shown as a molecular diagram with labeled atoms and bonds, including chlorine, fluorine, hydroxyl, and other functional groups as part of the quinolone antibiotic structure.*

FDA Label Image

Container Label (F3245022 7db4 463a A87c 550b4dc40201 02)

Moxifloxacin 0.5% ophthalmic solution label showing a 3 mL bottle. The label states the product is for ophthalmic use only and contains 5 mg/mL of moxifloxacin. It is manufactured by Lupin Limited, India, and marked as sterile for eye use.*

FDA Label Image

Carton Label (F3245022 7db4 463a A87c 550b4dc40201 03)

Moxifloxacin Ophthalmic Solution, USP 0.5% in a 3 mL bottle, labeled for prescription eye use only. The packaging includes storage instructions and ingredients, and notes that the product is sterile. Manufactured and distributed by Lupin Pharmaceuticals, with labeling indicating use for ocular administration.*

FDA Label Image

Image (F3245022 7db4 463a A87c 550b4dc40201 136 1)

Moxifloxacin 5 mg/mL ophthalmic solution/drops in a clear plastic bottle with a white child-resistant dropper cap. The bottle label shows the product name, strength, and usage route. The Redpharm Drug labeler name and NDC code 67296-2129 are visible on the packaging.*

* 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.