Pain Relieving Roll-on Gel
Product Images NDC 73842-001

2 FDA label images from Koi Cbd Llc · 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 Pain Relieving Roll-on Gel (NDC 73842-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Koi Cbd 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

Pain Relieving Roll-on Gel 6-pack Label (Pain Relieving Roll On Gel 6 Pack Label)

Pain Relieving Roll-on Gel 6-pack Label (Pain Relieving Roll On Gel 6 Pack Label)
Packaging label of Koi CBD Pain Relieving Roll-On Gel containing 500 mg CBD from broad spectrum hemp extract. The label features a blue icy background with the Koi CBD logo and states the product is a 3 fl. oz. (89 mL) roll-on gel. It includes a drug facts panel, barcode, QR code, labeler information (Koi CBD LLC, Norwalk, CA), and notes that the product is made in the USA and not tested on animals.*
FDA Label Image

Pain Relieving Roll-on Gel Label (Pain Relieving Roll On Gel Label)

Pain Relieving Roll-on Gel Label (Pain Relieving Roll On Gel Label)
Drug Facts panel from Koi CBD LLC's Pain Relieving Roll-On Gel containing 500 mg CBD per 3 fl. oz. bottle. Lists active ingredient as 10% menthol for cooling pain relief. Includes uses for minor aches, warnings about flammability and external use, directions for application, other storage info, and a detailed list of inactive ingredients including essential oils. Advises consulting a physician for children under 2 years or if conditions worsen. Made in the USA and not tested on animals.*

* 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.