Gentamicin Sulfate In Sodium Chloride Injection, Solution
Product Images NDC 0338-0511

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

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Gentamicin Sulfate In Sodium Chloride (NDC 0338-0511). 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

Gentamicin Structural Formula (Image 01)

Gentamicin Structural Formula (Image 01)
Chemical structure of Gentamicin Sulfate showing the molecular configuration and the three variants of the Gentamicin molecule (C1, C1A, C2) distinguished by the variable side group R as indicated in the accompanying key.*
FDA Label Image

Gentamicin Representative Container Label Ndc 0338-0507-41 (Image 02)

Gentamicin Representative Container Label Ndc 0338-0507-41 (Image 02)
Label for Gentamicin Sulfate in 0.9% Sodium Chloride Injection, 60 mg/50 mL (1.2 mg/mL) solution for intravenous use. The label includes cautions for intravenous use only, storage instructions, and manufacturer information from Baxter Healthcare Corporation, made in the USA.*
FDA Label Image

Gentamicin Serialization Carton Label 2b0851 (Image 03)

Gentamicin Serialization Carton Label 2b0851 (Image 03)
Label for Gentamicin Sulfate in 0.9% Sodium Chloride Injection 60 mg/50 mL solution. The label includes lot number T787987, expiration date August 2025, NDC 0338-0507-41, and quantity of 24 units of 50 mL. It features a barcode and a 2D matrix barcode. The labeler is Baxter Healthcare Corporation.*
FDA Label Image

Gentamicin Representative Container Label Ndc 0338-0509-41 (Image 04)

Gentamicin Representative Container Label Ndc 0338-0509-41 (Image 04)
Label for Gentamicin Sulfate in 0.9% Sodium Chloride Injection, 80 mg/50 mL (1.6 mg/mL) intravenous solution. The label includes cautions for intravenous use only, storage instructions at room temperature, and manufacturer details: Baxter Healthcare Corporation, Deerfield, IL, USA.*
FDA Label Image

Gentamicin Serialization Carton Label 2b0852 (Image 05)

Gentamicin Serialization Carton Label 2b0852 (Image 05)
Label for Gentamicin Sulfate in 0.9% Sodium Chloride Injection, 80 mg/50 mL solution for intravenous use. The lot number is T123456, with an expiration date of January 9999. The label includes a barcode, QR code, and other identification numbers. The quantity stated is 24 units of 50 mL each.*
FDA Label Image

Gentamicin Representative Container Label Ndc 0338-0505-48 (Image 06)

Gentamicin Representative Container Label  Ndc 0338-0505-48 (Image 06)
Label of Gentamicin Sulfate in 0.9% Sodium Chloride Injection showing a 100 mg/100 mL (1 mg/mL) intravenous solution. The label includes cautions for intravenous use, storage instructions, and indicates it is a sterile single-dose container. It is labeled by Baxter Healthcare Corporation, made in the USA.*
FDA Label Image

Gentamicin Serialization Carton Label 2b0863 (Image 07)

Gentamicin Serialization Carton Label 2b0863 (Image 07)
Label for Gentamicin Sulfate in 0.9% Sodium Chloride intravenous injection, 100 mg per 100 mL vial. The label includes lot number T123456, expiration date JAN 9999, barcode, and is produced by Baxter Healthcare Corporation.*
FDA Label Image

Gentamicin Representative Container Label Ndc 0338-0511-41 (Image 08)

Gentamicin Representative Container Label Ndc 0338-0511-41 (Image 08)
Label for Gentamicin Sulfate in 0.9% Sodium Chloride Injection, 100 mg/50 mL (2 mg/mL) solution for intravenous use. The label includes cautions for intravenous use only, storage instructions, and notes that it is a sterile single-dose container. Manufactured by Baxter Healthcare Corporation, Deerfield, IL, USA.*
FDA Label Image

Gentamicin Serialization Carton Label 2b0853 (Image 09)

Gentamicin Serialization Carton Label 2b0853 (Image 09)
Label for Gentamicin Sulfate in 0.9% Sodium Chloride injection, 100 mg per 50 mL solution. The label includes lot number T123456, expiration date JAN 9999, and a barcode with associated numeric identifiers. The product is intended for intravenous administration and is produced by Baxter Healthcare Corporation.*
FDA Label Image

Gentamicin Representative Carton Label Ndc 0338-0503-48 (Image 10)

Gentamicin Representative Carton Label  Ndc 0338-0503-48 (Image 10)
Label of Gentamicin Sulfate in 0.9% Sodium Chloride Injection, 80 mg/100 mL (0.8 mg/mL) intravenous solution. The label includes usage cautions, composition details, storage instructions, and states it is a sterile single dose container. Manufactured by Baxter Healthcare Corporation, Deerfield, IL, USA.*
FDA Label Image

Gentamicin Serialization Carton Label 2b0862 (Image 11)

Gentamicin Serialization Carton Label 2b0862 (Image 11)
Label for Gentamicin Sulfate in 0.9% Sodium Chloride Injection, 80 mg per 100 mL solution. The label shows lot number, expiration date, NDC 0338-0503-48, and includes barcodes. It indicates a quantity of 24 units of 100 mL. The product is by Baxter Healthcare Corporation.*
FDA Label Image

Gentamicin Representative Container Label 0338-0507-48 (Image 12)

Gentamicin Representative Container Label 0338-0507-48 (Image 12)
Label for Gentamicin Sulfate in 0.9% Sodium Chloride Injection, 120 mg/100 mL (1.2 mg/mL) intravenous solution by Baxter Healthcare Corporation. The label includes cautions for intravenous use, storage instructions, and states it is a sterile, single-dose container for prescription use only.*
FDA Label Image

Gentamicin Representative Carton Label 0338-0507-48 (Image 13)

Gentamicin Representative Carton Label 0338-0507-48 (Image 13)
Label for Gentamicin Sulfate in 0.9% Sodium Chloride injection, 120 mg/100 mL strength in solution form. The label shows lot number T123456, expiration date January 2000, code 2B0864, and quantity of 24-100 mL units. The label includes barcodes and the NDC number 0338-0507-48.*

* 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.