Hot/cold Menthol 16% Roll-on Liquid
Product Images NDC 82645-014

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 Hot/cold Menthol 16% Roll-on (NDC 82645-014). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pharma Nobis, 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

Freskaro Menthol Bottle 2026 (Freskaro Menthol Roll On Bottle 4 14 2026)

Freskaro Menthol Bottle 2026 (Freskaro Menthol Roll On Bottle 4 14 2026)
The product is Hot/Cold Menthol 16% Roll-On, a topical analgesic liquid with menthol 16% as the active ingredient. It is presented as a 2.5 fl oz (74 mL) roll-on applicator that is described as no mess, dries rapidly, and stain-free. The label includes directions, warnings, drug facts, and inactive ingredients, and is manufactured by Pharma Nobis, LLC in Texas. The packaging highlights comparison to a similar medicated no mess applicator.*
FDA Label Image

Freskaro Menthol Carton 2026 (Freskaro Menthol Roll On Carton 4 14 2026)

Freskaro Menthol Carton 2026 (Freskaro Menthol Roll On Carton 4 14 2026)
The label for Hot/Cold Menthol 16% Roll-On pain relieving liquid, a topical analgesic with 16 mg/100 mL menthol strength by Pharma Nobis, LLC. The packaging highlights a roll-on applicator, claims of no mess, rapid drying, and being stain-free. The front panel includes product size (2.5 fl oz or 74 mL), alongside warnings and inactive ingredient information on the side panels. A barcode and a red cross symbol are visible on the bottom right.*

* 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.