Naproxen Sodium Tablet, Film Coated
Product Images NDC 69230-329

View Photos of 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 69230-329). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Consumer Care 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

Naproxensodium-round-100s-cont-carton-label (Naproxensodium Round 100s Cont Carton Label)

Naproxensodium-round-100s-cont-carton-label (Naproxensodium Round 100s Cont Carton Label)
Packaging label for Naproxen Sodium Tablets USP, 220 mg (NSAID), a film-coated oral tablet. The label indicates 100 round shaped tablets, manufactured by Camber Consumer Care Inc. The label includes Drug Facts panels with usage directions, warnings, inactive ingredients, contact information, and storage instructions. The design features a blue gradient background with white text and the Camber Consumer Care logo.*
FDA Label Image

Naproxensodium-round-100s-cont-label (Naproxensodium Round 100s Cont Label)

Naproxensodium-round-100s-cont-label (Naproxensodium Round 100s Cont Label)
Packaging label for Naproxen Sodium Tablets USP 220 mg, round shaped, film-coated tablets. The label indicates 100 tablets per container and highlights the product as a pain reliever/fever reducer with strength to last 12 hours. Distributed by Camber Consumer Care, Inc., Piscataway, NJ. The label includes a barcode, an image of a tablet marked 'N11', and various warnings and directions on the reverse sides printed across multiple panels.*

* 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.