Oxacillin Injection, Solution
Product Images NDC 0338-1015

7 FDA label images from Baxter Healthcare Corporation · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Oxacillin (NDC 0338-1015). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Oxacillin Structural Formula (Image 01)

Oxacillin Structural Formula (Image 01)
Chemical structure of oxacillin, depicted as a molecular formula diagram showing the arrangement of atoms including a beta-lactam ring and side groups, with a water molecule (H2O) indicated.*
FDA Label Image

Oxacillin Representative Container Label (Image 02)

Oxacillin Representative Container Label (Image 02)
Label for Oxacillin Injection, USP by Baxter Healthcare Corporation, with a strength of 1 g per 50 mL single-dose container. The label includes product and manufacturer information, dosage form, storage instructions, and cautionary notes for intravenous use.*
FDA Label Image

Representative Carton Label 0338-1013-41 Panel 1 (Image 03)

Representative Carton Label 0338-1013-41 Panel 1 (Image 03)
Packaging label for OXACILLIN Injection, USP 1 g strength, presented in 12 - 50 mL single-dose containers. It is described as iso-osmotic with storage instructions not to store above -20°C (-4°F). The label features the Baxter logo and indicates Baxter Healthcare Corporation, Deerfield, IL, USA, as the labeler.*
FDA Label Image

Representative Carton Label 0338-1013-41 Panel 2 (Image 04)

Representative Carton Label 0338-1013-41 Panel 2 (Image 04)
OXACILLIN 2 g/50 mL solution in a GALAXY container by Baxter Healthcare Corporation. The label shows the NDC code 0338-1013-41 and instructions for intravenous use, including dosages, cautions, and solution details like osmolality adjustment and pH range of 6.5 to 8.5. The label features warnings about use in series connections and checking for leaks and sterility.*
FDA Label Image

Representative Container Label 0338-1015-41 (Image 05)

Representative Container Label 0338-1015-41 (Image 05)
Label for Oxacillin Injection, USP 2 g/50 mL by Baxter Healthcare Corporation. The single-dose container is 50 mL, iso-osmotic, sterile, and nonpyrogenic. The label includes dosing, storage, and handling information and emphasizes not forcing thaw by immersion or microwave. Made in USA.*
FDA Label Image

Representative Carton Label 0338-1015-41 (panel 1)

Representative Carton Label 0338-1015-41 (panel 1)
Packaging label for Oxacillin Injection, USP 2 g/50 mL by Baxter Healthcare Corporation. The label includes instructions for thawing and storage, emphasizing not to force thaw by immersion in water baths or microwave. It states the product is a single-dose, iso-osmotic solution and should not be stored below -20°C or frozen. The Baxter logo and manufacturer address in Deerfield, IL are also visible.*
FDA Label Image

Representative Carton Label 0338-1015-41 (panel 2)

Representative Carton Label 0338-1015-41 (panel 2)
Drug Facts and usage instructions for OXACILLIN 2 g/50 mL in GALAXY container by Baxter Healthcare Corporation. The label details the active ingredient as Oxacillin Sodium equivalent to 2.0 g Oxacillin with Dextrose Hydrous and Sodium Citrate Hydrous as buffers. It includes dosage instructions for intravenous use, cautionary statements on usage, and instructions on sterility and solution clarity.*

* 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.