Acetaminophen And Diphenhydramine Hydrochloride Tablet
Product Images NDC 58602-760

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 Acetaminophen And Diphenhydramine Hydrochloride (NDC 58602-760). 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.

FDA Label Image

Package Label-principal Display Panel 100 Caplets (Aurophen Fig1)

Package Label-principal Display Panel 100 Caplets (Aurophen Fig1)
The packaging label for Acetaminophen and Diphenhydramine Hydrochloride Gelcaps 500 mg/25 mg, an extra strength oral tablet product by Aurohealth LLC. The label highlights its use as a pain reliever and nighttime sleep aid, non-habit forming, rapid release formulation, and contains 20 gelcaps. The label includes Drug Facts in black text on a white background, usage instructions, warnings, and manufacturer information.*
FDA Label Image

Package Label-principal Display Panel 500 mg / 25 mg (20 Caplets Bottle Carton) (Aurophen Fig2)

Package Label-principal Display Panel 500 mg / 25 mg (20 Caplets Bottle Carton) (Aurophen Fig2)
Packaging label for Acetaminophen and Diphenhydramine Hydrochloride Gelcaps, extra strength 500 mg/25 mg, oral tablet form by Aurohealth LLC. The carton contains 20 gelcaps with a blue and red design featuring a crescent moon and stars. Label includes drug facts, warnings, usage instructions, inactive ingredients, barcode, and distributor information.*

* 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.