Asystem Radical Relief Gel Roll-on 300mg Cbd
Product Images NDC 52261-4901

2 FDA label images from Cosco International, Inc. · 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 Asystem Radical Relief Gel Roll-on 300mg Cbd (NDC 52261-4901). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosco International, 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

Bottle Label (Component Label)

Bottle Label (Component Label)
Label for ASYSTEM Radical Relief Gel Roll-On 300mg CBD by Cosco International, Inc. The label states the volume as 75ml (2.53 FL OZ) and highlights key points such as "Instant. Powerful. Maximum Absorption." Active ingredients include Menthol 10% and Menthyl Salicylate 16%, both external analgesics. Instructions indicate to roll gel onto painful areas until absorbed. The product is made in the USA and claims to contain CBD derived from USA-grown hemp, with certified THC-free content.*
FDA Label Image

Carton Label (Outer Carton)

Carton Label (Outer Carton)
Packaging label for ASYSTEM Radical Relief Gel Roll-On 300mg CBD by Cosco International, Inc. The light green box features the brand name ASYSTEM and highlights key benefits such as pain relief, inflammation reduction, joint mobility, sprains, arthritis, and stiffness. The label includes drug facts with active ingredients menthol 10% and methyl salicylate 15%, usage directions, warnings, inactive ingredients, and a QR code. The package size is 75ml (2.53 FL OZ), made in the USA, and provides contact information for questions.*

* 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.