Up And Up Naproxen Sodium Tablet, Film Coated
Product Images NDC 11673-909

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Up And Up Naproxen Sodium (NDC 11673-909). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target Corporation, 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 01

up and up naproxen sodium tablets, 220 mg film-coated tablets for oral use. The label states it is a pain reliever and fever reducer (NSAID), containing 100 caplets in a container with an easy-open arthritis cap and package not child-resistant. The label includes drug facts, directions, warnings, ingredients, and manufacturer information, with the Target Corporation as the labeler and NDC 11673-909.*

FDA Label Image

Image 02

Drug Facts panel continued for up and up naproxen sodium 220 mg tablets. It details warnings about when to stop use and consult a doctor, especially regarding signs of stomach bleeding, heart problems, stroke symptoms, or persistent side effects. It advises pregnant or breastfeeding individuals to consult a health professional before use. Directions specify dosing intervals and quantities for adults, children 12 years and older, and consultation advice for children under 12 years.*

* 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.