Pain Relief Roll-on Gel
Product Images NDC 72342-190

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Pain Relief Roll-on (NDC 72342-190). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by J.r. Watkins, 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

Principal Display Panel (85 g Bottle Label)

Principal Display Panel (85 g Bottle Label)
This is a pain relief roll-on that provides penetrating relief for muscle strains, soreness, and aching joints. It should be applied to the affected area not more than four times a day by massaging the painful area until it's absorbed into the skin. It is not for use on open wounds, damaged or irritated skin, and is not meant to be used with a heating pad or TENS device, or with any other creams, ointments, sprays, liniments, or other topical products containing camphor. It is for external use only, and contact with eyes or mucous membranes should be avoided. If you experience rash, itching, redness, or excessive irritation of the skin, stop using the product and consult a doctor. Pregnant or breastfeeding women should seek advice from a healthcare professional before using it. The product should be kept away from children and stored in dry, well-ventilated conditions at room temperature. The ingredients include arnica montana flower extract, cholecalciferol, denatured alcohol, ethylhexylglycerin, glycerin, hydroxyethylcellulose, magnesium chloride hexahydrate, Mentha piperita (peppermint) oil, phenoxyethanol, polysorbate 20, and water.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.