Cystex Max Strength Uti Pain Relief Tablet
Product Images NDC 69693-519

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cystex Max Strength Uti Pain Relief (NDC 69693-519). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clarion Brands 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

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Cystex Max Strength UTI Pain Relief oral tablet, brown, oblong shape with imprint "P99" on one side. The tablet is part of a product by Clarion Brands LLC with a strength of 99.5 mg/99.5 mg.*
FDA Label Image

Blister Label (Cystex Max Blister Label)

Blister Label (Cystex Max Blister Label)
The image shows multiple identical label sections for Cystex Max Strength UTI Pain Relief tablets. Each label includes the brand name Cystex LLC, location Chattanooga, TN 37403, active ingredient Phenazopyridine HCl 99.5 mg, placeholder lot and expiration numbers, and the designation MAXIMUM STRENGTH. The labels also feature the code RA/Drug/RAJ.-1750.*
FDA Label Image

Carton (Cystex Max Carton)

Carton (Cystex Max Carton)
The label for Cystex Max Strength UTI Pain Relief tablets features the product name prominently with active ingredient Phenazopyridine Hydrochloride 99.5 mg. It states fast-acting UTI pain relief targeting pain, burning, and urgency. The package contains 24 oral tablets, distributed by Clarion Brands LLC, with a blue and white design emphasizing relief within 15 minutes. The label includes Drug Facts, warnings, directions, inactive ingredients, a barcode, and contact 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.