Max Relief Junior Liquid
Product Images NDC 17856-0045

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 (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

Image Description (17856 0045 01)

Image Description (17856 0045 01)
Label for MAX relief junior acetaminophen oral elixir, 160 mg per 5 mL strength. The label indicates a bubble gum flavor, alcohol/aspirin/dye/sugar free formulation, with storage instructions and warnings. It includes dosage information stating delivery of 240 mg per 7.5 mL in a package of 48 syringes, distributed by Atlantic Biologicals Corp.*
FDA Label Image

Image Description (17856 0045 02)

Image Description (17856 0045 02)
Label for MAX relief junior acetaminophen oral elixir, 160 mg per 5 mL with a dosage of 40 mg per 1.25 mL. The label highlights bubble gum flavor, and states it is free of alcohol, aspirin, dyes, and sugar. The product is packaged as 120 syringes and distributed by Atlantic Biologicals Corp., Miami, FL. Storage instructions and safety warnings about keeping the medication out of children’s reach are included.*
FDA Label Image

Image Description (17856 0045 03)

Image Description (17856 0045 03)
Label for MAX relief junior Acetaminophen oral elixir, 160 mg per 5 mL delivering 80 mg per 2.5 mL dose. Bubble gum flavor, alcohol/aspirin/dye/sugar free. Packaged in 120 syringes by Unit Dose Solutions and distributed by Atlantic Biologicals Corp. Includes storage and safety instructions.*

* 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.