Max Relief Junior Liquid
Product Images NDC 17856-0025

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Max Relief Junior (NDC 17856-0025). 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

Image Description (17856 0025 01)

Label for MAX relief junior Acetaminophen oral elixir, 160 mg per 5 mL strength. The label indicates a dosage of 650 mg per 20.3 mL and specifies a bubble gum flavor. It is alcohol, aspirin, dye, and sugar free. The product is distributed by Atlantic Biologicals Corp., Miami, FL, and packaged in quantity of 50 cups. Additional storage and usage instructions are included.*

FDA Label Image

Image Description (17856 0025 03)

Label for MAX relief junior Acetaminophen oral elixir, 160 mg per 5 mL strength. This liquid medication is bubble gum flavored, alcohol, aspirin, dye, and sugar free. The label includes storage instructions, barcode, NDC number 17856-0025-03, and distributor Atlantic Biologicals Corp., Miami, FL. The package contains 72 cups and is marked for OTC use.*

FDA Label Image

Image Description (17856 0025 04)

Label for MAX relief junior Acetaminophen oral elixir, 160 mg per 5 mL, presented in 48 syringes. It is bubble gum flavored and alcohol/aspirin/dye/sugar free. Distributed by Atlantic Biologicals Corp. The label includes storage instructions and the product NDC 17856-0025.*

* 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.