Max Relief Junior Grape Liquid
Product Images NDC 17856-1122

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 Max Relief Junior Grape (NDC 17856-1122). 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

Image Description (17856 1122 01 Case Label)

Image Description (17856 1122 01 Case Label)
Label for MAX relief junior Grape flavor Children's Acetaminophen oral liquid, containing 160 mg per 5 mL, delivering 650 mg in 20.3 mL. The label indicates it is a grape-flavored pain reliever/fever reducer, alcohol/aspirin/dye free, with storage instructions and warnings. Packaged and distributed by Atlantic Biologicals Corp.*
FDA Label Image

Image Description (17856 1122 02 Case Label)

Image Description (17856 1122 02 Case Label)
Label for MAX relief junior Grape, a children's acetaminophen oral liquid with strength of 160 mg per 5 mL. The package delivers 40 mg per 1.25 mL and contains 120 enfit syringes. It is grape-flavored, alcohol, aspirin, and dye free. Labeled by Atlantic Biologicals Corp., Miami, FL.*
FDA Label Image

Image Description (17856 1122 04 Case Label)

Image Description (17856 1122 04 Case Label)
Label for MAX relief junior Grape Children's Acetaminophen oral liquid, containing 160 mg per 5 mL with a dosage of 480 mg per 15 mL. The grape-flavored liquid is marked as alcohol, aspirin, and dye-free, and is packaged in 72 cups. Distributed by Atlantic Biologicals Corp.*

* 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.