Metoclopramide Solution
Product Images NDC 17856-1190

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoclopramide (NDC 17856-1190). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals 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.

Product Images & Figures Index

FDA Label Image

1 (17856 1190 01 Rev. 1 Case Label)

1 (17856 1190 01 Rev. 1 Case Label)
Label for Metoclopramide HCl Oral Solution USP 5 mg per 5 mL, a human prescription drug in oral liquid form. The label indicates the product is alcohol/sugar free with vanilla flavor, supplied in a quantity of 72 cups. Distributed by Atlantic Biologicals Corp., Miami, FL, it includes storage instructions and a barcode with GTIN and expiration date.*
FDA Label Image

2 (17856 1190 02 Rev. 1 Case Label)

2 (17856 1190 02 Rev. 1 Case Label)
Label for Metoclopramide HCl oral solution, USP, 5 mg per 5 mL (delivers 1 mg/mL), packaged as 120 ENFIT syringes. The label states metoclopramide 5 mg is present as hydrochloride, with alcohol/sugar free vanilla flavor, stored at 20-25°C, and includes manufacturer Atlantic Biologicals Corp., Miami, FL. Features include GTIN barcode and expiration date of 08/22/25.*
FDA Label Image

Fae3363a-figure-01 (Fae3363a Figure 01)

Fae3363a-figure-01 (Fae3363a Figure 01)
Chemical structure of Metoclopramide, showing its molecular composition including chlorine, amine, methoxy, and methyl groups, along with associated hydrochloride (HCl) and water (H2O) molecules.*

* 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.