NDC Package 44911-0501-1 Lyme HP

Baptisia Tinctoria,Echinacea (angustifolia),Hydrastis Canadensis,Borrelia Burgdorferi - 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:
44911-0501-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Lyme HP
Non-Proprietary Name:
Baptisia Tinctoria, Echinacea (angustifolia), Hydrastis Canadensis, Borrelia Burgdorferi Nosode, Babesia Microti, Ehrlichia Nosode (canine), Meningococcus Nosode, Hepatitis B Nosode, Arsenicum Album, Bryonia (alba), Chelidonium Majus, Colchicum Autumnale, Kalmia Latifolia, Ledum Palustre, Lycopodium Clavatum, Phosphorus, Rhus Tox
Substance Name:
Arsenic Trioxide; Babesia Microti; Baptisia Tinctoria Root; Borrelia Burgdorferi; Bryonia Alba Root; Chelidonium Majus; Colchicum Autumnale Bulb; Echinacea Angustifolia; Ehrlichia Canis; Goldenseal; Hepatitis B Virus; Kalmia Latifolia Leaf; Ledum Palustre Twig; Lycopodium Clavatum Spore; Neisseria Meningitidis; Phosphorus; Toxicodendron Pubescens Leaf
Usage Information:
May temporarily relieve symptoms associated with infections, such asĀ aches and pains of joints and muscles.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve symptoms associated with infections, such as aches and pains of joints and muscles.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
11-Digit NDC Billing Format:
44911050101
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:
    07-11-2019
    End Marketing Date:
    08-07-2024
    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 44911-0501-1?

    The NDC Packaged Code 44911-0501-1 is assigned to a package of 30 ml in 1 bottle, dropper of Lyme 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 44911-0501 included in the NDC Directory?

    Yes, Lyme HP with product code 44911-0501 is active and included in the NDC Directory. The product was first marketed by Energique, Inc. on July 11, 2019.

    What is the 11-digit format for NDC 44911-0501-1?

    The 11-digit format is 44911050101. 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
    5-4-144911-0501-15-4-244911-0501-01