Gr Arthritis Pain Relief Roll-on 1500 Mg
Product Images NDC 78232-005

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gr Arthritis Pain Relief Roll-on 1500 Mg (NDC 78232-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clarity Labs 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

Ifc Label (Gr 1500 1)

Packaging label for GR Arthritis pain relief roll-on 1500 mg by Clarity Labs LLC. The label highlights temporary relief of minor aches and pains associated with arthritis using camphor 4% and menthol 8%. It includes botanical extracts like black cohosh, chickweed, comfrey leaf, devil’s claw, evening primrose flower, and horsetail grass. The label states max strength and 1500 mg added CBD. Directions, warnings, and an NDC code 78232-005-002 are also visible.*

FDA Label Image

Tube Label (Gr 1500 2)

Drug facts panel for GR Arthritis pain relief roll-on 1500 mg by Clarity Labs LLC. It lists active ingredients camphor 4% and menthol 8% as topical analgesics, and details uses for temporary relief of minor aches and pains related to arthritis, strains, sprains, backaches, and bruises. Includes inactive ingredients, warnings, directions for adult use, product size 3 fl oz, and manufacturer information.*

FDA Label Image

Outer Box (Gr 1500 3)

Packaging label for GR Arthritis pain relief roll-on 1500 mg by Clarity Labs LLC. The label features a gradient teal to green background with the product name prominently displayed. It includes details on pain relief for arthritis, formulary extracts such as menthol and camphor, and a barcode. The label specifies a roll-on delivery system with 4 units per package and the Green Roads brand logo.*

* 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.