Prochlorperazine Edisylate Injection
Product Images NDC 70069-371

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Prochlorperazine Edisylate (NDC 70069-371). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, Llc, 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

Image (80fcf53c 6832 4ff6 88d2 D6cb588048bf 01)

Chemical structure of prochlorperazine edisylate showing its molecular components, including a chlorinated phenothiazine ring and sulfonic acid groups, consistent with the active ingredient prochlorperazine edisylate.*

FDA Label Image

Container Label (80fcf53c 6832 4ff6 88d2 D6cb588048bf 02)

Label for Prochlorperazine Edisylate Injection, USP, 10 mg/2 mL (5 mg/mL) in a 2 mL multiple-dose vial. Intended for deep intramuscular or intravenous use only, not for subcutaneous use. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL. Storage instructions specify 20° to 25°C with permitted excursions, and protect from light. Includes barcode and manufacturing details.*

FDA Label Image

Carton Label (80fcf53c 6832 4ff6 88d2 D6cb588048bf 03)

Packaging label for Prochlorperazine Edisylate Injection, USP 10 mg/2 mL (5 mg/mL) in multiple-dose vials. It is manufactured for Somerset Therapeutics, LLC. The label includes dosage strength, route of administration (intramuscular and intravenous), storage instructions, and a barcode. The label states the product is for prescription use only.*

FDA Label Image

Carton Label (80fcf53c 6832 4ff6 88d2 D6cb588048bf 04)

Label for Prochlorperazine Edisylate Injection, USP, 10 mg/2 mL (5 mg/mL), manufactured for Somerset Therapeutics, LLC. The product is supplied as 10 x 2 mL multiple-dose vials, intended for deep intramuscular or intravenous use only. The label includes storage instructions, composition details, a barcode, and a note that it is Rx only.*

* 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.