Mens Spectral Uhp Extra Strength Hair Regrowth Treatment
Product Images NDC 69188-001

View Photos of 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 Mens Spectral Uhp Extra Strength Hair Regrowth Treatment (NDC 69188-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ds Healthcare Group, Inc., 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

Box 1 (Spectral.uhp 1 Month Box)

Box 1 (Spectral.uhp 1 Month Box)
Packaging label for Mens SPECTRAL UHP Extra Strength Hair Regrowth Treatment by DS Healthcare Group, Inc. The label includes detailed Drug Facts listing minoxidil 5% topical solution as the active ingredient, usage instructions, warnings, and directions. The front panel highlights the product as an unscented, 60 mL (2 FL OZ) one-month supply topical solution for men to reactivate hair follicles and help regrow hair, not for use by women. The label also includes company information, a barcode, and instructions for patent use and storage.*
FDA Label Image

Box 3 (Spectral.uhp 3 Month Box)

Box 3 (Spectral.uhp 3 Month Box)
Mens SPECTRAL UHP EXTRA STRENGTH HAIR REGROWTH TREATMENT carton packaging by DS Healthcare Group, Inc. Front panel displays the product name with 5% minoxidil topical solution for hair regrowth. The box highlights that it is a 3-month supply containing three 60 mL (2 FL OZ) bottles. The side panels include Drug Facts, usage directions, warnings, and company contact information. The design features blue, black, gray, and silver color accents and embossed details.*

* 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.