NDC Package 44911-0538-1 Arthritis HP

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:
44911-0538-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Arthritis HP
Non-Proprietary Name:
Apis Mellifica, Bryonia (alba), Causticum, Colchicum Autumnale, Kali Carbonicum, Kalmia Latifolia, Ledum Palustre, Pulsatilla (pratensis), Rhododendron Chrysanthum, Rhus Tox
Substance Name:
Anemone Pratensis; Apis Mellifera; Bryonia Alba Root; Causticum; Colchicum Autumnale Bulb; Kalmia Latifolia Leaf; Ledum Palustre Twig; Potassium Carbonate; Rhododendron Aureum Leaf; Toxicodendron Pubescens Leaf
Usage Information:
May temporarily relieve symptoms due to minor joint inflammation and swelling.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve symptoms due to minor joint inflammation and swelling.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
11-Digit NDC Billing Format:
44911053801
Product Type:
Human Otc Drug
Labeler Name:
Energique, Inc.
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:
    03-25-2020
    End Marketing Date:
    04-16-2025
    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 44911-0538-1?

    The NDC Packaged Code 44911-0538-1 is assigned to a package of 30 ml in 1 bottle, dropper of Arthritis HP, a human over the counter drug labeled by Energique, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 44911-0538 included in the NDC Directory?

    Yes, Arthritis HP with product code 44911-0538 is active and included in the NDC Directory. The product was first marketed by Energique, Inc. on March 25, 2020.

    What is the 11-digit format for NDC 44911-0538-1?

    The 11-digit format is 44911053801. 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
    5-4-144911-0538-15-4-244911-0538-01