Pain Release Granule
Product Images NDC 70983-004

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pain Release (NDC 70983-004). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Saje Natural Business 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

Image Description (Pain Release 120g Bath Salt Envelope Usa Final R1 01)

Packaging label for Pain Release 1.6 mg/g Menthol topical granules by Saje Natural Business Inc. The label identifies the product as a pain relieving bath salt soak with a net weight of 4.2 oz (120 g). The back panel includes drug facts, active ingredient, uses, warnings, directions, and inactive ingredients.*

FDA Label Image

Image Description (Pain Release 620g Bath Salt Bottle Usa Final R1 01)

Drug Facts label for Pain Release topical granules containing Menthol 0.16% as the active ingredient, serving as an external analgesic. The label includes uses for temporary relief of pain and itching, warnings for external use only, directions for use by adults and children 12 years and older, and a list of inactive ingredients such as various essential oils and salts. Packaging states the product is made by Saje Natural Business Inc. in Canada and weighs 21.9 oz (620 g).*

FDA Label Image

Painrelease 300g Bath Salt Tub 705607 Usa Final

Drug Facts label panel for Pain Release pain relieving bath salt soak by Saje Natural Business Inc, containing Menthol 0.16% as the active ingredient for external analgesic use. The label includes uses, warnings, directions for adults and children, inactive ingredients, storage instructions, and manufacturer contact information.*

* 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.