Ibuprofen And Diphenhydramine Citrate Tablet, Coated
Product Images NDC 58602-867

2 FDA label images from Aurohealth 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 Ibuprofen And Diphenhydramine Citrate (NDC 58602-867). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth 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.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (200 mg/38 mg (20 Coated Caplets) Bottle Label)

Package Label-principal Display Panel (200 mg/38 mg (20 Coated Caplets) Bottle Label)
Drug facts and warnings for Ibuprofen and Diphenhydramine Citrate tablets 200 mg/38 mg by Aurohealth LLC. The label includes active ingredients' purposes, allergy and stomach bleeding warnings, usage instructions, dosage directions, inactive ingredients list, and contact information for questions or comments. It displays a lot and expiration placeholder for printing.*
FDA Label Image

Package Label-principal Display Panel (200 mg/38 mg (20 Coated Caplets) Bottle Carton Label)

Package Label-principal Display Panel (200 mg/38 mg (20 Coated Caplets) Bottle Carton Label)
The packaging label for Ibuprofen and Diphenhydramine Citrate Tablets, 200 mg/38 mg, by Aurohealth LLC. The label shows a 20 count bottle of coated caplets, combining a pain reliever (NSAID) and nighttime sleep-aid. It includes Drug Facts panels with active ingredients, uses, warnings, inactives, and directions. The packaging also displays the NDC 58602-867-73 and barcode, with the product distributed by Aurohealth LLC and made in India.*

* 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.