Ciprofloxacin Otic Solution/ Drops
Product Images NDC 64950-381

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Ciprofloxacin Otic (NDC 64950-381). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Genus Lifesciences, 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

Chemical Structure (Cipro 01)

Chemical structure of Ciprofloxacin hydrochloride monohydrate, showing a quinolone core with a fluorine substitution, cyclopropyl group, piperazine ring, and associated hydrochloride and water molecules.*

FDA Label Image

Image (Cipro 02)

An instructional illustration showing hands washing with soap and water, emphasizing proper hand hygiene technique.*

FDA Label Image

Image (Cipro 03)

Illustration depicting the proper method for administering ear drops, showing a hand holding an ear and a dropper positioned above for instillation.*

FDA Label Image

Image (Cipro 04)

Black-and-white instructional diagram showing how to apply Ciprofloxacin Otic solution. The left image depicts a person tilting their head to the side exposing the ear, while the right image illustrates a hand pulling the ear back and upward to prepare for instilling the drops into the ear canal.*

FDA Label Image

Principal Display Panel (14 Vial Carton)

Label for Ciprofloxacin Otic Solution 0.2%, an auricular solution containing 0.5 mg ciprofloxacin per 0.25 mL. The label notes the product is sterile, preservative-free, for ear use only, and contains 14 single-dose 0.25 mL containers. Manufactured by Genus Lifesciences Inc., with packaging by Holopack Verpackungstechnik in Germany. Includes storage instructions, barcode, and Rx only designation.*

* 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.