Tobramycin And Dexamethasone Suspension/ Drops
Product Images NDC 0574-4031

4 FDA label images from Padagis Us Llc · 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 0574-4031). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Padagis Us Llc, 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

Tobramycin (Image 01)

Tobramycin (Image 01)
Chemical structure diagram showing a detailed molecular structure likely representing the active ingredient in the product, tobramycin and dexamethasone ophthalmic suspension/drops by Padagis US LLC.*
FDA Label Image

Dexamethasone (Image 02)

Dexamethasone (Image 02)
Chemical structure diagram of dexamethasone, an active ingredient in the tobramycin and dexamethasone ophthalmic suspension/drops by Padagis US LLC.*
FDA Label Image

Serialization (Image 03)

Serialization (Image 03)
A text panel showing placeholders for product serialization details including serial number (S/N), lot number (Lot), and expiration date (Exp) for the product Tobramycin and Dexamethasone ophthalmic suspension/drops by Padagis US LLC.*
FDA Label Image

Tob-dex-ctn-10-19 (Tob Dex Ctn 10 19)

Tob-dex-ctn-10-19 (Tob Dex Ctn 10 19)
Packaging label for Tobramycin and Dexamethasone Ophthalmic Suspension, USP 0.3%/0.1%, a sterile ophthalmic suspension for topical use only. The label shows NDC 0574-4031-25, indicates a 2.5 mL bottle size, and lists Padagis US LLC as the labeler with manufacturing in Greece. It includes active ingredient concentrations, preservative details, storage instructions, and a barcode.*

* 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.