Dragon Pain Relieving Balm
Product Images NDC 83552-114

View Photos of 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 Dragon Pain Relieving Balm (NDC 83552-114). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Americanna Wellness, 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

1 (83552 114 00 Dragon 3.4 Rollup Xtra Isolate Carton)

1 (83552 114 00 Dragon 3.4 Rollup Xtra Isolate Carton)
Dragon Pain Relieving Balm packaging label by AMERICANNA WELLNESS, INC. The label features a black and gold design with a dragon illustration and states 'Xtra Strength' and 'Isolate Menthol 11% | Camphor 10%'. It highlights 1000 mg CBD content and nano emulsified cannabinoids for enhanced bioavailability. The net weight is 3.4 oz (96.4 g). The label includes a Drug Facts section with active ingredients Camphor 10% and Menthol 11%, uses, warnings, directions, inactive ingredients, and manufacturer contact information.*
FDA Label Image

2 (83552 114 00 Dragon 3.4 Rollup Xtra Isolate Inner)

2 (83552 114 00 Dragon 3.4 Rollup Xtra Isolate Inner)
Label of Dragon Pain Relieving Balm by AMERICANNA WELLNESS, INC. It features active ingredients Menthol 11% and Camphor 10%, highlighting nano emulsified cannabinoids for 3x faster bioavailability. The label includes product weight of 3.4 oz (96.4 g) and usage, warnings, directions, inactive ingredients, and manufacturer information in a decorative design with a dragon motif.*

* 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.