Max Relief Junior Liquid
Product Images NDC 17856-0045

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 Max Relief Junior (NDC 17856-0045). 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

1 (17856 0045 01 Rev. 2 Label)

1 (17856 0045 01 Rev. 2 Label)
Label for MAX relief junior Children's Acetaminophen Oral Elixir, 160 mg per 5 mL, packaged as 48 syringes. The label indicates the product is bubble gum flavored, alcohol/aspirin/dye free, and includes storage instructions and safety warnings. Distributed by Atlantic Biologicals Corp.*
FDA Label Image

2 (17856 0045 02 Rev. 2 Label)

2 (17856 0045 02 Rev. 2 Label)
Label for MAX relief junior Children's Acetaminophen Oral Elixir, 160 mg per 5 mL liquid dosage form. The label states it delivers 40 mg per 1.25 mL, is bubble gum flavored, and free of alcohol, aspirin, and dyes. It is distributed by Atlantic Biologicals Corp., Miami, FL, and the package contains 120 syringes.*
FDA Label Image

3 (17856 0045 03 Rev. 2 Label)

3 (17856 0045 03 Rev. 2 Label)
Label for MAX relief junior Children's Acetaminophen Oral Elixir, containing 160 mg per 5 mL with a dosage delivering 80 mg per 2.5 mL. The product is bubble gum flavored, alcohol/aspirin/dye free, and intended for oral use. It is distributed by Atlantic Biologicals Corp. and includes a quantity of 120 Enfit syringes. Storage instructions specify room temperature protection from freezing and light, with a warning to keep out of reach of children.*

* 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.