Monistat Maintain Tablet
Product Images NDC 63736-020

1 FDA label image from Insight Pharmaceuticals Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Monistat Maintain (NDC 63736-020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Insight Pharmaceuticals 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

Maintain™ From The Makers Of Monistat® A Trusted Leader In Feminine Care (logo)uti2-in-1 Test + Pain Relief Kitphenazopyridine HCl 99.5 mg / Urinary Analgesicwith Cranberry Flavored Coating 2 Uti Test Strips | 12 Urinary Pain Relief Tablets (Monistat Maintain 63736 020 12 01)

Maintain™ From The Makers Of Monistat® A Trusted Leader In Feminine Care (logo)uti2-in-1 Test + Pain Relief Kitphenazopyridine HCl 99.5 mg / Urinary Analgesicwith Cranberry Flavored Coating 2 Uti Test Strips | 12 Urinary Pain Relief Tablets (Monistat Maintain 63736 020 12 01)
The Monistat Maintain UTI 2-in-1 Test + Pain Relief Kit packaging label features the proprietary name prominently with the active ingredient Phenazopyridine HCl 99.5 mg noted as a urinary analgesic. The label highlights the kit includes 2 UTI test strips and 12 cranberry-flavored urinary pain relief tablets, marketed for fast temporary relief of pain, burning, and urgency. The labeler is Insight Pharmaceuticals LLC with product NDC 63736-020. Instructions, drug facts, and warnings are provided on the back panel.*

* 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.