Multiple Vitamins (adult) Single Dose Kit
Product Images NDC 60505-6172

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Multiple Vitamins (adult) Single Dose (NDC 60505-6172). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotex Corp, 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

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Packaging label for Multiple Vitamins Injection (Adult), sterile kit by Apotex Corp. The label lists contents as five vials each of 5 mL (Vial 1 and Vial 2) for intravenous infusion, with each vial to be used once and discarded. Active ingredients for each 5 mL vial are detailed, including Vitamin C 200 mg, Vitamin A 3,300 IU, and others. The label includes storage instructions and manufacturer information for Gland Pharma Limited (Hyderabad, India) and Apotex Corp. (Weston, Florida).*

FDA Label Image

Vial1.jpg (Vial1)

Label for Multiple Vitamins Injection (Adult) Vial 1, a sterile single-dose vial for intravenous infusion. The vial must be diluted before use and contains storage and usage instructions, including refrigeration and light protection. Manufactured for Apotex Corp in Hyderabad, India. The label also includes a barcode and space for lot and expiration information.*

FDA Label Image

Vial2.jpg (Vial2)

Label for Multiple Vitamins Injection (Adult) Vial 2, sterile single-dose vial for intravenous infusion. The label indicates it must be diluted before use and discarded if unused. It is manufactured for Apotex Corp, Hyderabad, India, and includes storage instructions to keep refrigerated between 2°C to 8°C (36°F to 46°F) and protect from light.*

* 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.