Ascor Injection
Product Images NDC 67157-101

7 FDA label images from Mcguff Pharmaceuticals, Inc. · 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 Ascor (NDC 67157-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mcguff Pharmaceuticals, Inc., 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

Serialization Block (Pi 2d Barcode)

Serialization Block (Pi 2d Barcode)
Ascor 500 mg/mL injection vial label by McGuff Pharmaceuticals, Inc. The label includes the proprietary name Ascor and the generic name Ascorbic Acid, indicating it is for intravenous use. The label displays volume and concentration information along with a barcode and lot numbers for identification.*
FDA Label Image

Formula (Ascorbic Acid Molecular Formula)

Formula (Ascorbic Acid Molecular Formula)
Chemical structure of ascorbic acid (Vitamin C), showing the arrangement of hydroxyl groups and carbon atoms in the molecule. This structure is associated with the active ingredient in Ascor injection 500 mg/mL by McGuff Pharmaceuticals, Inc.*
FDA Label Image

Pi_page_1.jpg (Pi Page 1)

Pi_page_1.jpg (Pi Page 1)
This image shows the prescribing information highlights for Ascor (ascorbic acid injection) 500 mg/mL for intravenous use, including indications, dosage and administration instructions, contraindications, warnings, precautions, adverse reactions, and drug interactions. It includes dosage recommendations by patient population, detailed preparation steps, and handling guidelines supplied by McGuff Pharmaceuticals, Inc., revised in January 2024.*
FDA Label Image

Pi_page_2.jpg (Pi Page 2)

Pi_page_2.jpg (Pi Page 2)
This is a detailed drug package insert for Ascor (ascorbic acid) injection, USP 500 mg/mL, 50 mL vial from McGuff Pharmaceuticals, Inc. The insert includes sections on adverse reactions, drug interactions, use in specific populations, clinical pharmacology with a chemical structure diagram of ascorbic acid, nonclinical toxicology, storage, and patient counseling information. It provides comprehensive prescribing information as required by FDA labeling.*
FDA Label Image

Tray Pack.jpg (Tray Pack)

Tray Pack.jpg (Tray Pack)
Label for Ascor (Ascorbic Acid Injection, USP) 500 mg/mL (25,000 mg/50 mL) intravenous injection, manufactured by McGuff Pharmaceuticals, Inc. The label indicates a pharmacy bulk package of 25 vials, each 50 mL, with NDC 67157-101-51. It includes storage instructions, usage directions, and a barcode.*
FDA Label Image

Vial Carton.jpg (Vial Carton)

Vial Carton.jpg (Vial Carton)
Carton label for Ascor (Ascorbic Acid Injection, USP) 500 mg/mL injection, 50 mL single vial, manufactured by McGuff Pharmaceuticals, Inc. The label states a total of 25,000 mg per 50 mL vial and includes handling instructions such as protecting from light, refrigeration recommendations, and warnings about pressure development. The label notes the product is a pharmacy bulk package not for direct infusion, for intravenous use only, and contains no preservative.*
FDA Label Image

Vial Label.jpg (Vial Label)

Vial Label.jpg (Vial Label)
Label for Ascor (Ascorbic Acid Injection, USP) 500 mg/mL in a 50 mL vial by McGuff Pharmaceuticals, Inc. The label states the concentration as 25,000 mg/50 mL and includes storage instructions, warnings, and a barcode. It is labeled as a Pharmacy Bulk Package for intravenous use only, with no preservatives and specific handling precautions.*

* 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.