Natural Relief Arthritis Therapy Tablet, Orally Disintegrating
Product Images NDC 17312-437

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 Natural Relief Arthritis Therapy (NDC 17312-437). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Trp Company, 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

Package Label (Arthritis Therapy Screenshot 2025 11 12)

Package Label (Arthritis Therapy Screenshot 2025 11 12)
Natural Relief Arthritis Therapy orally disintegrating tablets by TRP Company. The homeopathic product features 70 fast dissolving tablets formulated with natural active ingredients for joint pain, stiffness, immobility, and swelling. The label highlights gluten-free status and detailed drug facts, including active and inactive ingredients, directions, warnings, and contact information.*
FDA Label Image

Bottle Label (Arthritis Therapy Screenshot 2025 11 12 Bottle)

Bottle Label (Arthritis Therapy Screenshot 2025 11 12 Bottle)
Label for Natural Relief Arthritis Therapy fast dissolving tablets by TRP Company. The label lists active homeopathic ingredients including Acetylsalicylic acid, Apis mellifica, Bryonia alba, Calcarea fluorica, Lithium carbonicum, Rhus tox, and Ruta graveolens at various HPUS potencies. It states the product contains 70 tablets, provides usage warnings and directions, inactive ingredients, and manufacturer contact information. The label includes a tamper-evident seal warning and notes the product is homeopathic and gluten-free.*

* 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.