Moxifloxacin Ophthalmic Solution Solution/ Drops
Product Images NDC 67296-2222

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 Moxifloxacin Ophthalmic Solution (NDC 67296-2222). 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

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

Structure (22d5cd84 26c0 49b0 Afbf 1e9155749cf6 01)
Chemical structure diagram of moxifloxacin, displaying its molecular components and bonds as labeled in the image.*
FDA Label Image

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

Bottle Label (22d5cd84 26c0 49b0 Afbf 1e9155749cf6 02)
Moxifloxacin Ophthalmic Solution USP 0.5% sterile solution for topical ophthalmic use, 3 mL vial. Label indicates prescription use only, manufactured for Lifestar Pharma LLC, made in India. Includes storage instructions, active ingredient moxifloxacin hydrochloride 5.45 mg per mL (equivalent to 5 mg moxifloxacin). Features barcode and lot/expiration placeholders.*
FDA Label Image

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

Bottle Carton (22d5cd84 26c0 49b0 Afbf 1e9155749cf6 03)
Packaging label for Moxifloxacin Ophthalmic Solution, USP 0.5% sterile solution in 3 mL size by Lifestar, a product manufactured for Lifestar Pharma LLC. The label includes active ingredient details, storage instructions, and usage for topical ophthalmic use only. The design features the NDC 70756-638-25 and includes barcodes and manufacturing 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.