Vancomycin Hydrochloride Injection, Solution
Product Images NDC 0338-3580

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

Product Visual Gallery

This gallery contains 31 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 0338-3580). 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

Vancomycin Hydrochloride Structural Formula (Image 01)

Vancomycin Hydrochloride Structural Formula (Image 01)
Chemical structure diagram of vancomycin hydrochloride, showing the detailed molecular arrangement of the antibiotic compound including its distinctive aromatic rings, hydroxyl groups, and amino acid side chains.*
FDA Label Image

Vancomycin Representative Container Label Ndc 0338-3551-48 (Image 02)

Vancomycin Representative Container Label Ndc 0338-3551-48 (Image 02)
Vancomycin Injection, USP in 5% Dextrose, 500 mg per 100 mL (5 mg/mL) solution for injection. Single-dose container labeled GALAXY by Baxter Healthcare Corporation. The label includes storage instructions, dosage form as injection, and cautions for intravenous use only.*
FDA Label Image

Vancomycin Representative Carton Label Ndc 0338-3551-48 Panel 1 Of 3 (Image 03)

Vancomycin Representative Carton Label Ndc 0338-3551-48 Panel 1 Of 3 (Image 03)
Text panel providing storage and handling instructions for VANCOMYCIN HYDROCHLORIDE injection solution, including thawing at room temperature or refrigeration, warnings against thawing by immersion in water baths or microwave irradiation, chemical stability duration in GALAXY plastic containers, and caution about freezing and fragility of product containers.*
FDA Label Image

Vancomycin Representative Carton Label Ndc 0338-3551-48 Panel 2 Of 3 (Image 04)

Vancomycin Representative Carton Label Ndc 0338-3551-48 Panel 2 Of 3 (Image 04)
Vancomycin Injection, USP 500 mg per 100 mL (5 mg/mL) in 5% Dextrose, depicted in packaging label text. The label states it contains 6 single-use bags, each 100 mL. Storage instructions specify to keep at or below -20°C/-4°F. The labeler is Baxter Healthcare Corporation, with NDC 0338-3551-48 and code 2G3551, for Rx only.*
FDA Label Image

Vancomycin Representative Carton Label Ndc 0338-3551-48 Panel 3 Of 3 (Image 05)

Vancomycin Representative Carton Label Ndc 0338-3551-48 Panel 3 Of 3 (Image 05)
Text panels labeled GALAXY Container provide drug information for Vancomycin Hydrochloride Injection, Solution, 500 mg/100 mL strength. The nonsterile solution contains vancomycin hydrochloride, USP equivalent to 500 mg vancomycin, along with 5 g dextrose hydrous in water for injection. Instructions include intravenous use only, caution against adding supplements or additives, and mention prescribing information. Manufacturer is Baxter Healthcare Corporation, Deerfield, IL USA.*
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Vancomycin Representative Container Label 0338-3552-48 (Image 06)

Vancomycin Representative Container Label 0338-3552-48 (Image 06)
A printed label panel showing placeholder text for manufacturing details including code, lot number, expiration date, quantity, and serial number. Two identical sections each contain a square labeled 'FOR PLACEMENT ONLY', with strings of placeholder alphanumeric codes below. The label includes GS1 barcode application identifiers.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3552-48 Panel 1 Of 3 (Image 07)

Vancomycin Representative Carton Label 0338-3552-48 Panel 1 Of 3 (Image 07)
Label for Vancomycin Injection, USP in 5% Dextrose, strength 1 g per 200 mL (5 mg/mL), single-dose container by Baxter Healthcare Corporation. The label details storage instructions, dosage form as injection solution, intravitreal route, and cautions for intravenous use only. It lists ingredients and handling instructions including temperature storage and thawing guidance.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3552-48 Panel 2 Of 3 (Image 08)

Vancomycin Representative Carton Label 0338-3552-48 Panel 2 Of 3 (Image 08)
This text panel provides thawing and storage instructions for a pharmaceutical product in a GALAXY plastic container (PL 2040). It states the product should be thawed at room temperature (25°C/77°F) or under refrigeration (5°C/41°F), not thawed by water baths or microwave, and not refrozen. The solution remains stable for 72 hours at room temperature or 30 days refrigerated. It also advises careful handling of frozen containers due to fragility.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3552-48 Panel 3 Of 3 (Image 09)

Vancomycin Representative Carton Label 0338-3552-48 Panel 3 Of 3 (Image 09)
Vancomycin Injection, USP in 5% Dextrose, 1 g per 200 mL (5 mg/mL) injection solution for intravitreal use. The label indicates the product is prescription only, supplied as 3 single-use bags each containing 200 mL. Storage is advised at or below -20°C/-4°F. Label includes NDC 0338-3552-48 and Baxter Healthcare Corporation as the labeler.*
FDA Label Image

Vancomycin Representative Container Label 0338-3580-48 (Image 10)

Vancomycin Representative Container Label 0338-3580-48 (Image 10)
Drug text panel for VANCOMYCIN HYDROCHLORIDE injection solution shows contents per 100 mL, including 500 mg vancomycin hydrochloride and 5 g dextrose hydrous in water for injection. It states the product is sterile, nonpyrogenic, for intravenous use only, with dosage and caution notes referenced to prescribing information. Labeler is Baxter Healthcare Corporation, Deerfield, IL.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3580-48 Panel 1 Of 3 (Image 11)

Vancomycin Representative Carton Label 0338-3580-48 Panel 1 Of 3 (Image 11)
A label panel displaying placeholder text fields for product code, lot number, expiration date, quantity, and serial number. The phrase 'FOR PLACEMENT ONLY.' appears inside a square box twice, indicating a template layout for a vial or carton label, without specific drug information shown.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3580-48 Panel 2 Of 3 (Image 12)

Vancomycin Representative Carton Label 0338-3580-48 Panel 2 Of 3 (Image 12)
Label for Vancomycin Injection, USP in 5% Dextrose, with strength 750 mg per 150 mL (5 mg/mL). It is a single-dose container by Baxter Healthcare Corporation, intended for intravenous use with instructions for storage and handling. The label includes cautions, storage temperature guidelines, and proprietary names Galaxy and Baxter.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3580-48 Panel 3 Of 3 (Image 13)

Vancomycin Representative Carton Label 0338-3580-48 Panel 3 Of 3 (Image 13)
A storage and handling instruction panel for Vancomycin Hydrochloride injection solution. It details thawing conditions at room temperature or refrigeration, warnings against thawing by immersion or microwave irradiation, stability durations for the thawed solution in Galaxy plastic containers, and advises against refreezing. It also cautions handling frozen product containers with care due to fragility.*
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Vancomycin Representative Container Label 0338-3581-01 (Image 14)

Vancomycin Representative Container Label 0338-3581-01 (Image 14)
Label for Vancomycin Injection, USP 750 mg per 150 mL (5 mg/mL) in 5% Dextrose, presented as three single-use bags each containing 150 mL. The label indicates storage instructions and includes an NDC number 0338-3580-48 with associated barcode position information. The product is for prescription use only by Baxter Healthcare Corporation.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3581-01 Panel 1 Of 3 (Image 15)

Vancomycin Representative Carton Label 0338-3581-01  Panel 1 Of 3 (Image 15)
Label for VANCOMYCIN HYDROCHLORIDE injection solution, showing two identical text sections describing a 100 mL GALAXY container formulation. Each 100 mL contains 500 mg vancomycin hydrochloride with 5 g dextrose hydrous in water for injection, USP. The label notes intravenous use, cautions against adding medication or additives, and includes Baxter Healthcare Corporation as the labeler with trademark information.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3581-01 Panel 2 Of 3 (Image 16)

Vancomycin Representative Carton Label 0338-3581-01  Panel 2 Of 3 (Image 16)
This image shows a label for Vancomycin Hydrochloride injection solution by Baxter Healthcare Corporation. The label includes placeholder text for lot number, expiration date, quantity, and serial number. It also features a boxed area labeled 'FOR PLACEMENT ONLY' and coding lines with partially obscured identifiers, likely for serialization and traceability purposes.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3581-01 Panel 3 Of 3 (Image 17)

Vancomycin Representative Carton Label 0338-3581-01  Panel 3 Of 3 (Image 17)
Label for Vancomycin Injection, USP 500 mg per 100 mL (5 mg/mL) in 0.9% Sodium Chloride by Baxter Healthcare Corporation. The label states this is a sterile, nonpyrogenic, single-dose container for intravenous use only. It includes storage instructions and cautions about thawing and handling, with the brand name Galaxy also mentioned.*
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Vancomycin Representative Container Label 0338-3582-01 (Image 18)

Vancomycin Representative Container Label 0338-3582-01 (Image 18)
This text panel provides storage and handling instructions for Vancomycin Hydrochloride injection, solution in GALAXY plastic containers. It advises thawing at room temperature or under refrigeration, warns against thawing by immersion in water baths or microwaves, and specifies the solution's chemical stability durations at different temperatures. It cautions to avoid force thawing and re-freezing, and notes the fragility of frozen product containers.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3582-01 Panel 1 Of 3 (Image 19)

Vancomycin Representative Carton Label 0338-3582-01 Panel 1 Of 3 (Image 19)
Vancomycin Injection USP in 0.9% Sodium Chloride, 500 mg per 100 mL (5 mg/mL) solution for injection. Label shows a box containing 6 single-dose bags, each with 100 mL. Storage instructions indicate to store at or below -20°C/-4°F. The label features NDC 0338-3581-01 and is marked Rx Only.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3582-01 Panel 2 Of 3 (Image 20)

Vancomycin Representative Carton Label 0338-3582-01  Panel 2 Of 3 (Image 20)
This image shows a text panel from a Vancomycin Hydrochloride injection solution labeled as a GALAXY Container by Baxter Healthcare Corporation. It lists ingredients for each 100 mL, including vancomycin hydrochloride equivalent to 500 mg vancomycin and sodium chloride in Water for Injection. It includes dosage instructions for intravenous use only and cautions against adding supplementary medications or additives. Manufacturer information for Baxter Healthcare Corporation is also displayed.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3582-01 Panel 3 Of 3 (Image 21)

Vancomycin Representative Carton Label 0338-3582-01  Panel 3 Of 3 (Image 21)
This image shows a labeling panel for VANCOMYCIN HYDROCHLORIDE injection, solution for intravitreal use by Baxter Healthcare Corporation. The label includes placeholder fields for code, lot number, expiration date, quantity, and serial number, and features standardized barcode information. It is a duplicate label likely intended for product placement on packaging.*
FDA Label Image

Vancomycin Representative Container Label 0338-3583-01 (Image 22)

Vancomycin Representative Container Label 0338-3583-01 (Image 22)
Vancomycin Injection, USP in 0.9% Sodium Chloride, 750 mg per 150 mL (5 mg/mL) solution for injection. Single-dose container labeled GALAXY by Baxter Healthcare Corporation. Intravitreal route indicated, with storage instructions and dosage cautions visible.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3583-01 Panel 1 Of 3 (Image 23)

Vancomycin Representative Carton Label 0338-3583-01  Panel 1 Of 3 (Image 23)
Text panel with thawing and handling instructions for the product in PL 2040 Plastic containers, specifying temperature conditions for thawing and storage, warnings against thawing by immersion in water baths or microwave, and advisories for careful handling of frozen containers due to fragility.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3583-01 Panel 2 Of 3 (Image 24)

Vancomycin Representative Carton Label 0338-3583-01  Panel 2 Of 3 (Image 24)
Label for Vancomycin Injection USP 750 mg per 150 mL (5 mg/mL) in 0.9% Sodium Chloride, provided as three single-dose bags each containing 150 mL. The label includes storage instructions to keep the product iso-osmotic at or below -20°C/-4°F. It is marked as Rx Only and shows an NDC of 0338-3582-01 from Baxter Healthcare Corporation.*
FDA Label Image

Vancomycin Representative Carton Label 0338-3583-01 Panel 3 Of 3 (Image 25)

Vancomycin Representative Carton Label 0338-3583-01  Panel 3 Of 3 (Image 25)
This image shows two identical text panels for Baxter Healthcare Corporation's Vancomycin Hydrochloride injection solution. Each panel details that each 100 mL contains vancomycin hydrochloride equivalent to 500 mg vancomycin, along with sodium chloride in water for injection. It states sterile, nonpyrogenic conditions, dosage instructions for intravenous use only, and cautions against adding supplementary medication or additives. The panels display the Baxter logo and company address in Deerfield, IL.*
FDA Label Image

Image 26

Image 26
Label for VANCOMYCIN HYDROCHLORIDE injection solution, intravitreal route. The label includes placeholder text for lot number, expiration date, quantity, and serial number. It also contains a boxed area marked 'FOR PLACEMENT ONLY' and various coded identifiers. The label is from Baxter Healthcare Corporation.*
FDA Label Image

Image 27

Image 27
Label for Vancomycin Injection, USP 1 g per 200 mL (5 mg/mL) in 0.9% Sodium Chloride, intraveneous use, single-dose container by Baxter Healthcare Corporation. The label includes storage instructions, contents per 100 mL, and cautions not to freeze or add supplements. It also specifies nonpyrogenic, iso-osmotic formulation and Rx only status.*
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Image 28

Image 28
This text panel provides storage and handling instructions for a frozen pharmaceutical product in PL 2040 plastic containers, advising thawing at room temperature or refrigeration, avoiding microwave or water bath thawing, and cautioning that product containers may be fragile when frozen. It notes chemical stability durations under different conditions and explicitly states not to refreeze the product.*
FDA Label Image

Image 29

Image 29
Label for Vancomycin Injection, USP in 0.9% Sodium Chloride, 1 g per 200 mL (5 mg/mL) solution. The label states it contains three single-dose bags, each with 200 mL, and advises storing at or below -20°C (-4°F). It is labeled RX Only with NDC 0338-3583-01 and code 2G3592. The labeler is Baxter Healthcare Corporation.*
FDA Label Image

Image 30

Image 30
Drug facts text panel for Vancomycin Hydrochloride Injection, Solution in a GALAXY container. It states each 100 mL contains 500 mg vancomycin hydrochloride with sodium chloride in water for injection. The solution is sterile, nonpyrogenic, and intended for intravenous use only. Cautions advise against adding supplementary medication or additives. The labeler is Baxter Healthcare Corporation, Deerfield, IL.*
FDA Label Image

Image 31

Image 31
This image shows a text panel likely from a label or packaging insert, including placeholder fields for code, lot number, expiration date, quantity, and serial number. It includes the text 'FOR PLACEMENT ONLY.' twice, each within a box, suggesting a template or mock-up format.*

* 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.