NDC Package 71742-0002-1 Arthri-joint T008

Apis Mellifica,Bryonia (alba),Causticum,Colchicum Autumnale,Kali Carbonicum,Kalmia - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
71742-0002-1
Package Description:
59 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Arthri-joint T008
Non-Proprietary Name:
Apis Mellifica, Bryonia (alba), Causticum, Colchicum Autumnale, Kali Carbonicum, Kalmia Latifolia, Ledum Palustre, Pulsatilla (vulgaris), Rhododendron Chrysanthum, Rhus Tox
Substance Name:
Apis Mellifera; Bryonia Alba Root; Causticum; Colchicum Autumnale Bulb; Kalmia Latifolia Leaf; Ledum Palustre Twig; Potassium Carbonate; Pulsatilla Vulgaris; Rhododendron Aureum Leaf; Toxicodendron Pubescens Leaf
Usage Information:
May temporarily relieve symptoms due to minor joint inflammation and swelling. May temporarily relieve symptoms due to minor joint inflammation and swelling.
11-Digit NDC Billing Format:
71742000201
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Renuma Medical Systems Co., Ltd
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(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    10-19-2017
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 71742-0002-1?

    The NDC Packaged Code 71742-0002-1 is assigned to a package of 59 ml in 1 bottle, dropper of Arthri-joint T008, a human over the counter drug labeled by Guangzhou Renuma Medical Systems Co., Ltd. The product's dosage form is liquid and is administered via oral form.

    Is NDC 71742-0002 included in the NDC Directory?

    Yes, Arthri-joint T008 with product code 71742-0002 is active and included in the NDC Directory. The product was first marketed by Guangzhou Renuma Medical Systems Co., Ltd on October 19, 2017 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 71742-0002-1?

    The 11-digit format is 71742000201. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-171742-0002-15-4-271742-0002-01