Sunmark Arthritis Pain Reliever
Product Images NDC 49348-921

2 FDA label images from Sunmark · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sunmark Arthritis Pain Reliever (NDC 49348-921). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sunmark, 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

This Is The 100 Count Bottle Label For Sunmark Apap Arthritis. (Apap 100)

This Is The 100 Count Bottle Label For Sunmark Apap Arthritis. (Apap 100)
Label for Sunmark Arthritis Pain Reliever featuring acetaminophen extended-release tablets, each 650 mg. The label states relief for minor arthritis pain and fever reduction, includes warnings, and lists uses. It indicates the package contains 100 caplets and emphasizes tamper-evident packaging.*
FDA Label Image

This Is The 50 Count Bottle Carton Label For Sunmark Apap Arthritis. (Apaparthritis)

This Is The 50 Count Bottle Carton Label For Sunmark Apap Arthritis. (Apaparthritis)
Sunmark Arthritis Pain Reliever Acetaminophen Extended-Release Tablets, USP 650 mg carton label featuring the Sunmark brand. It contains 50 caplets, each 650 mg, described as pain reliever and fever reducer for temporary relief of minor arthritis pain. The label highlights that the effect lasts up to 8 hours and includes a depiction of a white capsule-shaped tablet. Additional drug facts and warnings are printed on the label.*

* 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.