Keranique Hair Regrowth Treatment For Women Spray
Product Images NDC 70550-578

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Keranique Hair Regrowth Treatment For Women (NDC 70550-578). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Profectus Beauty, 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

1-month (Keranique 1 Month)

Carton packaging for KERANIQUE Hair Regrowth Treatment For Women, a 2% minoxidil topical solution spray in a 60 mL (2 fl oz) bottle, distributed by International Hair Institute. The label highlights the FDA approval, product purpose as hair regrowth treatment for women, usage instructions, warnings, and features a precision sprayer image. The packaging uses dark maroon, gray, black, and yellow colors.*

FDA Label Image

2-month (Keranique 2 Month)

Packaging label for KERANIQUE Hair Regrowth Treatment For Women, 2% Minoxidil Topical Solution USP, in spray dosage form. The label displays FDA approval, usage instructions, warnings, and a two-month supply with two 60 mL bottles. The labeler is Profectus Beauty, LLC. The design includes hair regrowth claims and images illustrating the treatment area on the scalp.*

FDA Label Image

3-month (Keranique 3 Month)

Packaging label for KERANIQUE Hair Regrowth Treatment For Women, a 2% minoxidil topical solution spray. The label is maroon and white, manufactured by Profectus Beauty, LLC, and includes Drug Facts, directions, and warnings. The package is a three-month supply containing three 60 mL bottles with a precision sprayer. It is FDA approved and intended for topical use on the scalp to regrow hair on women with general thinning at the vertex.*

* 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.