Sombra Plus Cbd 500mg Cool Therapy
Product Images NDC 61577-7500

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Sombra Plus Cbd 500mg Cool Therapy (NDC 61577-7500). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sombra Cosmetics 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

Label (Sombra Plus Cbd 500mg Cool Therapy)

Drug Facts panel for Sombra Plus CBD 500MG Cool Therapy gel. Lists menthol USP 6.0% as active ingredient, classified as an external analgesic. Describes uses for temporary relief of minor muscle and joint aches related to strains, bruises, and sprains. Includes warnings about external use only, avoidance on wounds or damaged skin, and precautions for pregnant or breastfeeding users. Directions specify application frequency for adults and children over 2 years with a note to consult a doctor for younger children. Inactive ingredients and customer service contact information are also provided.*

* 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.