The Solu Tion Aerosol, Foam
Product Images NDC 82617-110

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for The Solu Tion (NDC 82617-110). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Scalp Tech 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

Pdp (1786116743521 405b6751 9286 4eec 8cc7 7a7b21007f42 1)

Label for THE SOLUTION topical anesthetic foam containing lidocaine and epinephrine. The label features a dark background with stylized blue wings and text indicating the product is a topical anesthetic. The package size is 1.7 fl oz (50 mL). The label includes manufacturer SCALP TECH INC and an instruction to use a maximum of 4 times daily.*

FDA Label Image

Dfp (1786116743521 405b6751 9286 4eec 8cc7 7a7b21007f42 2)

Drug Facts panel for THE SOLU TION topical aerosol foam containing 5% lidocaine hydrochloride and 0.01% epinephrine hydrochloride. It provides active ingredients, uses, warnings, directions, other information, inactive ingredients, and contact information in both English and French. The product is manufactured by Scalp Tech Inc in the USA.*

* 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.