Geri-tussin
Product Images NDC 17856-0693

3 FDA label images from Atlantic Biologicals Corp. · 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 Geri-tussin (NDC 17856-0693). 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.

FDA Label Image

17856 0693 01 (label)

17856 0693 01 (label)
Label for Geri-Tussin (Guaifenesin) oral solution, USP, 200 mg per 10 mL, packaged as 72 cups. The label includes storage instructions to keep at 15°-30°C (59°-86°F), protect from light and freezing, and notes it is sugar and alcohol free. It is labeled as an expectorant and is an over-the-counter (OTC) product distributed by Atlantic Biologicals Corp.*
FDA Label Image

17856 0693 02

17856 0693 02
Label for Geri-Tussin (Guaifenesin) oral solution, USP, 300 mg per 15 mL dose. The package contains 50 cups intended for unit dose administration. It is sugar and alcohol free and classified as an expectorant. The label includes storage instructions, a barcode, lot number, expiration date, and contact information for reorder. Packaged by Unit Dose Solutions and distributed by Atlantic Biologicals Corp.*
FDA Label Image

17856 0693 03 (label)

17856 0693 03 (label)
Geri-Tussin (Guaifenesin) oral solution label showing 100 mg/5 mL strength. The label notes storage instructions, sugar/alcohol free, quantity of 72 cups, and over-the-counter status. Packaged by Unit Dose Solutions and distributed by Atlantic Biologicals Corp. Contact reorder phone number included.*

* 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.