Naproxen Sodium
Product Images NDC 68016-661

2 FDA label images from Pharmacy Valuce Alliance, Llc · 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 Naproxen Sodium (NDC 68016-661). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pharmacy Valuce Alliance, Llc, 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

50 Count (300000023 Pv Naproxen 50ct Tablets Carton R2 Approved)

50 Count (300000023 Pv Naproxen 50ct Tablets Carton R2 Approved)
Packaging label for Naproxen Sodium Tablets USP 220 mg from Pharmacy Valuce Alliance, LLC. The label indicates the product is a pain reliever and fever reducer, gluten-free with strength lasting 12 hours, containing 50 tablets. The label includes Drug Facts panels with usage information, inactive ingredients, and warnings, as well as barcodes and manufacturing details.*
FDA Label Image

100 Count (300000025 Pv Naproxen 100ct Tablets Carton R2 Approved)

100 Count (300000025 Pv Naproxen 100ct Tablets Carton R2 Approved)
Packaging label for Naproxen Sodium Tablets USP 220 mg by Pharmacy Valuce Alliance, LLC. The label specifies 100 tablets in the package and identifies the product as a pain reliever/fever reducer. The design includes dosage information and drug facts panels with warnings, inactive ingredients, and usage instructions. The label also shows the UPC barcode and states that the product is gluten-free with strength lasting up to 12 hours.*

* 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.