Max Relief Junior Liquid
Product Images NDC 71399-0020

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 71399-0020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akron Pharma Inc., 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

16oz (16oz)

16oz (16oz)
MAX relief junior Children's Acetaminophen Oral Liquid, 160 mg per 5 mL, dye-free, cherry flavor. The label features dosage instructions by age and weight for children 2 to 11 years, warnings, inactive ingredients, and manufacturer Akron Pharma Inc. The 16 fl. oz. (473 mL) bottle label also includes a smiling child image and emphasizes it is an alcohol- and aspirin-free pain reliever and fever reducer.*
FDA Label Image

4oz (4oz)

4oz (4oz)
MAX relief junior Children's Acetaminophen Oral Liquid 160 mg per 5 mL, Cherry flavor, dye-free, alcohol and aspirin free. The front of the 4 FL.OZ (118 mL) label features colorful text, dosage information, and a photo of a child with an excited expression. The label states it is for ages 2 to 11 years and includes the Akron Pharma logo. The back panels include detailed drug facts, uses, warnings, dosing instructions by weight and age, and inactive ingredients.*
FDA Label Image

8oz (8oz)

8oz (8oz)
MAX relief junior Children's Acetaminophen Oral Liquid, 160 mg per 5 mL, Cherry flavor, 8 FL.OZ (236 mL) bottle. Dye-Free, Alcohol Free, Aspirin Free. Labeled for ages 2 to 11 years. Manufactured by Akron Pharma Inc., featuring a child's photo on the label. Includes dosing chart by age and weight and Tamper Evident warnings.*

* 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.