Naproxen Sodium And Diphenhydramine Hcl Tablet, Film Coated
Product Images NDC 62207-814

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Naproxen Sodium And Diphenhydramine Hcl (NDC 62207-814). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules India Ltd, 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

Carton

Packaging label for Naproxen Sodium and Diphenhydramine HCl 220 mg/25 mg film-coated caplet tablets by Granules India Ltd. The label includes Drug Facts detailing active ingredients, uses for occasional sleeplessness with minor aches and pains, warnings, directions, and other information. The package is child-resistant and the product is oral dosage form.*

FDA Label Image

Label

Packaging label for Naproxen Sodium and Diphenhydramine HCl Tablets 220 mg/25 mg, film-coated caplet tablets by Granules India Ltd. The label includes active ingredient strengths, use as a pain reliever and nighttime sleep-aid, caplet count of 500, and manufacturer information. The design features dosing warnings, drug facts, and storage instructions.*

FDA Label Image

Nap-diphen-label1-jpg (Nap Diphen Label1 Jpg)

Label for Naproxen Sodium 220 mg and Diphenhydramine Hydrochloride 25 mg tablets, film coated. Label includes batch number, manufacturing date, expiration date, manufacturing license number, NDC 62207-814-38, storage conditions (20°C to 25°C), and country of origin (India). The tablets are packaged with a quantity of 5 x 7500 tablets, with associated weights and box number also noted.*

FDA Label Image

Nap-diphen-label2-jpg (Nap Diphen Label2 Jpg)

This is a label for Naproxen Sodium 220 mg and Diphenhydramine Hydrochloride 25 mg film-coated tablets. The label includes batch number, manufacturing and expiration dates as placeholders, manufacturing license number, NDC code 62207-814-39, storage instructions at 20°C to 25°C, and a caution for repacking only. The product is labeled as originating from India and contains 7500 tablets.*

* 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.