Dragon Pain Relieving Balm
Product Images NDC 83552-113

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 83552-113). 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 113 00 Dragon 3.4 Rollup Regular Full Spectrum Carton)

1 (83552 113 00 Dragon 3.4 Rollup Regular Full Spectrum Carton)
The packaging label for Dragon Pain Relieving Balm by AMERICANNA WELLNESS, INC. features a red background with a gold dragon graphic. It is labeled as regular strength and full spectrum with 5.3% menthol, 3.1% camphor, 500 mg CBD, 30 mg CBN, and 30 mg CBG. The net weight is 3.4 oz (96.4 g). The label includes Drug Facts with active ingredients camphor and menthol, usage, warnings, directions, and inactive ingredients. It also highlights 3x faster bioavailability with nano emulsified cannabinoids, and terpene profile percentages for nerolidol, myrcene, pinene, humulene, and caryophyllene. The manufacturer's information and barcode are shown at the bottom.*
FDA Label Image

2 (83552 113 00 Dragon 3.4 Rollup Regular Full Spectrum Inner)

2 (83552 113 00 Dragon 3.4 Rollup Regular Full Spectrum Inner)
Dragon Pain Relieving Balm packaging label shows a 3.4 oz (96.4g) container from AMERICANNA WELLNESS, INC. The label highlights active ingredients Menthol 5.3% and Camphor 3.1%, with a traditional dragon graphic and red background. Features include nano emulsified cannabinoids for enhanced bioavailability and detailed Drug Facts and usage warnings.*

* 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.