Tobramycin And Dexamethasone Suspension/ Drops
Product Images NDC 24208-295

4 FDA label images from Bausch & Lomb Incorporated · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tobramycin And Dexamethasone (NDC 24208-295). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bausch & Lomb Incorporated, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

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The image shows a warning statement panel that reads: "DO NOT USE IF IMPRINTED NECKBAND IS NOT INTACT." This is likely a tamper-evident caution related to the product packaging for Tobramycin and Dexamethasone ophthalmic suspension/drops.*
FDA Label Image

Image 01

Image 01
Chemical structure diagram of the active ingredient Tobramycin. The image shows the molecular structure with oxygen, nitrogen, and hydroxyl groups clearly depicted, illustrating Tobramycin's aminoglycoside antibiotic composition.*
FDA Label Image

Image 02

Image 02
Chemical structure of dexamethasone, one of the active ingredients in Tobramycin and Dexamethasone ophthalmic suspension/drops by Bausch & Lomb Incorporated.*
FDA Label Image

Image 03

Image 03
Packaging label for Tobramycin and Dexamethasone Ophthalmic Suspension, USP 0.3%/0.1% (sterile) by Bausch & Lomb Incorporated. The label includes dosage form suspension drops, volume 10 mL, with directions to shake well and storage instructions. The label states it is for ophthalmic use only and prescription use (Rx only). Active ingredients are Tobramycin 3 mg/mL and Dexamethasone 1 mg/mL.*

* 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.