Nuvarra Mens Minoxidil Hair Regrowth Treatment Solution
Product Images NDC 87779-966

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nuvarra Mens Minoxidil Hair Regrowth Treatment (NDC 87779-966). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bionetics Health 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

Inner Package (Inner Package)

Label for Nuvarra Mens Minoxidil Hair Regrowth Treatment 5% topical solution, 60 mL bottle. The label states it is a men's extra strength, unscented topical solution to reactivate hair follicles and stimulate regrowth. It includes usage instructions, warnings, inactive ingredients, storage conditions, and distributor information for Nuvarra Labs.*

FDA Label Image

Label Insert (Label Insert)

This image shows the detailed patient information leaflet for Nuvarra Mens Minoxidil Hair Regrowth Extra Strength 5% Minoxidil Topical Solution. It covers usage instructions, expected results, safety warnings, precautions, and application directions with an illustration of the dropper applicator. The leaflet advises on hair regrowth expectations and emphasizes proper application for men only.*

FDA Label Image

Outer Package (Outer Package)

Nuvarra Mens Minoxidil Hair Regrowth Treatment 5% topical solution carton showing branding and product details. The label states it contains one 60 mL (2 fl oz) bottle with a child-resistant dropper applicator. It is marketed for men to treat hair loss on the top of the scalp (vertex only). The product is unscented, made in the USA by Nuvarra Labs, and not for use by women. Warnings, directions, and drug facts panels are partially visible on the carton.*

* 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.