Arthritis Pain And Joint Relief Liquid
NDC Package 57955-9982-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Arthritis Pain And Joint Relief (actaea spicata, aesculus hippocastanum, arnica montana, bellis perennis, bryonia, calcarea carbonica, calcarea fluorica, causticum, cimicifuga racemosa, formicum acidum, hypericum perforatum, ledum palustre, lithium carbonicum, magnesia phosphorica, phosphorus, phytolacca decandra, pulsatilla, rhododendron chrysanthum, rhus tox, ruta graveolens, salicylicum acidum, sepia and zincum metallicum.) liquids is uses † For temporary relief of:backacheleg crampsstiff swollen jointsirritabilitysore tendons and ligamentsbody acheship and knee discomfortsfatiguerestless limbs† Claims based on traditional Homeopathic practice, not acceptedmedical evidence, not FDA evaluated. This formulation utilizes a liquid delivery system. Marketed by King Bio Inc., this product is identified by NDC 57955-9982.

Identification & Billing

NDC Package Code
57955-9982-2
Package Description
59 mL in 1 BOTTLE, SPRAY
Product Code
57955-9982
11-Digit Billing Format
57955998202

Clinical Specifications

Proprietary Name
Arthritis Pain And Joint Relief
Non-Proprietary Name
Actaea Spicata, Aesculus Hippocastanum, Arnica Montana, Bellis Perennis, Bryonia, Calcarea Carbonica, Calcarea Fluorica, Causticum, Cimicifuga Racemosa, Formicum Acidum, Hypericum Perforatum, Ledum Palustre, Lithium Carbonicum, Magnesia Phosphorica, Phosphorus, Phytolacca Decandra, Pulsatilla, Rhododendron Chrysanthum, Rhus Tox, Ruta Graveolens, Salicylicum Acidum, Sepia And Zincum Metallicum.
Substance Name
Actaea Spicata Root; Arnica Montana Whole; Bellis Perennis Whole; Black Cohosh; Bryonia Alba Root; Calcium Fluoride; Causticum; Formic Acid; Horse Chestnut; Hypericum Perforatum Whole; Lithium Carbonate; Magnesium Phosphate, Dibasic Trihydrate; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Phytolacca Americana Root; Pulsatilla Vulgaris Whole; Rhododendron Aureum Leaf; Rhododendron Tomentosum Leafy Twig; Ruta Graveolens Flowering Top; Salicylic Acid; Sepia Officinalis Juice; Toxicodendron Pubescens Leaf; Zinc
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Uses † For temporary relief of:backacheleg crampsstiff swollen jointsirritabilitysore tendons and ligamentsbody acheship and knee discomfortsfatiguerestless limbs† Claims based on traditional Homeopathic practice, not acceptedmedical evidence, not FDA evaluated.

Regulatory & Marketing

Labeler Name
King Bio Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-10-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 57955-9982-2 identifies a specific commercial package of 59 ml in 1 bottle, spray of Arthritis Pain And Joint Relief, a human over the counter drug labeled by King Bio Inc.. This liquid is formulated for oral use and contains actaea spicata root; arnica montana whole; bellis perennis whole; black cohosh; bryonia alba root; calcium fluoride; causticum; formic acid; horse chestnut; hypericum perforatum whole; lithium carbonate; magnesium phosphate, dibasic trihydrate; oyster shell calcium carbonate, crude; phosphorus; phytolacca americana root; pulsatilla vulgaris whole; rhododendron aureum leaf; rhododendron tomentosum leafy twig; ruta graveolens flowering top; salicylic acid; sepia officinalis juice; toxicodendron pubescens leaf; zinc as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by King Bio Inc. on March 10, 2026. The current certification is valid through December 31, 2027.

How is this King Bio Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 57955998202. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
57955-9982-2
11-Digit CMS (5-4-2)
57955-9982-02

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.