Moxifloxacin Hydrochloride Solution/ Drops
Product Images NDC 67296-2232

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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 Hydrochloride (NDC 67296-2232). 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 (1a4f432a C2b2 46bc 88fc 7379c2bbd0a2 01)

Structure (1a4f432a C2b2 46bc 88fc 7379c2bbd0a2 01)
Chemical structure diagram of Moxifloxacin Hydrochloride, illustrating its molecular components and arrangement as an ophthalmic solution active ingredient.*
FDA Label Image

Image (1a4f432a C2b2 46bc 88fc 7379c2bbd0a2 02)

Image (1a4f432a C2b2 46bc 88fc 7379c2bbd0a2 02)
Label for Moxifloxacin Ophthalmic Solution USP 0.5%, 3 mL vial, sterile ophthalmic drops. Contains 5.45 mg moxifloxacin hydrochloride per mL (equivalent to 5 mg moxifloxacin). For topical ophthalmic use only. Storage instructions: 2°C to 25°C. Manufactured for Somerset Therapeutics, LLC, Somerset, NJ; made in India.*
FDA Label Image

Image (1a4f432a C2b2 46bc 88fc 7379c2bbd0a2 03)

Image (1a4f432a C2b2 46bc 88fc 7379c2bbd0a2 03)
Label for Moxifloxacin Ophthalmic Solution, USP 0.5% (5 mg/mL) in a 3 mL sterile solution/drops format. It shows the drug is Rx only with active ingredient moxifloxacin hydrochloride equivalent to 5 mg moxifloxacin per mL. Manufactured for Somerset Therapeutics LLC, the label includes storage instructions and tamper-evident seal notice, featuring the Somerset Therapeutics logo.*

* 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.