Dragon Pain Relieving Balm
Product Images NDC 83552-112

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 83552-112). 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.

Product Images & Figures Index

FDA Label Image

1 (83552 112 00 Dragon 2.0 Jar Xtra Full Spectrum Carton)

1 (83552 112 00 Dragon 2.0 Jar Xtra Full Spectrum Carton)
Packaging label for Dragon Pain Relieving Balm by AMERICANNA WELLNESS, INC. The balm includes full spectrum cannabinoids with 600mg CBD, 150mg CBN, 50mg CBG, and less than 0.3% THC. The label highlights ingredients menthol 11% and camphor 10% as topical analgesics and a terpene profile of 20% each: nerolidol, myrcene, pinene, humulene, and caryophyllene. The net weight is 2 oz (56.7g), and the label features directions, warnings, inactive ingredients, and drug facts.*
FDA Label Image

2 (83552 112 00 Dragon 2.0 Jar Xtra Full Spectrum Inner)

2 (83552 112 00 Dragon 2.0 Jar Xtra Full Spectrum Inner)
The image shows the packaging label for Dragon Pain Relieving Balm Xtra Strength by AMERICANNA WELLNESS, INC. The balm contains menthol 11% and camphor 10% and comes in a 2 oz (56.7 g) container. The label highlights '3x Faster Bioavailability' with nano emulsified cannabinoids and features a dragon graphic. Manufactured by AMERICANNA WELLNESS INC., located in Bellingham, WA.*

* 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.