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  5. NDC Package Code: 55714-4848-1 Hbp

NDC Package 55714-4848-1 Hbp

Ruta Graveolens,Valeriana Officinalis,Adrenalinum,Arsenicum Iodatum,Aurum - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
55714-4848-1
Package Description:
30 mL in 1 BOTTLE, GLASS
Product Code:
55714-4848
Proprietary Name:
Hbp
Non-Proprietary Name:
Ruta Graveolens, Valeriana Officinalis, Adrenalinum, Arsenicum Iodatum, Aurum Metallicum, Baryta Carbonica, Bryonia, Cactus Grandiflorus, Chelidonium Majus, Cinchona Officinalis, Crotalus Horridus, Digitalis Purpurea, Glonoinum, Kali Carbonicum, Kali Iodatum, Lachesis Mutus, Naja Tripudians, Nux Vomica, Veratrum Album, Vipera Berus, Viscum Album, Elaps Corallinus.
Substance Name:
Arsenic Triiodide; Barium Carbonate; Bryonia Alba Root; Chelidonium Majus; Cinchona Officinalis Bark; Crotalus Horridus Horridus Venom; Digitalis; Epinephrine; Gold; Lachesis Muta Venom; Micrurus Corallinus Venom; Naja Naja Venom; Nitroglycerin; Potassium Carbonate; Potassium Iodide; Ruta Graveolens Flowering Top; Selenicereus Grandiflorus Stem; Strychnos Nux-vomica Seed; Valerian; Veratrum Album Root; Vipera Berus Venom; Viscum Album Fruiting Top
Usage Information:
Formulated for associated symptoms such as headache, ear ringing, anxiety, sweating, pallor and nausea.
11-Digit NDC Billing Format:
55714484801
Product Type:
Human Otc Drug
Labeler Name:
Newton Laboratories, 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.
    • Active Ingredient(s):
  • ARSENIC TRIIODIDE 15 [hp_X]/mL
  • BARIUM CARBONATE 15 [hp_X]/mL
  • BRYONIA ALBA ROOT 15 [hp_X]/mL
  • CHELIDONIUM MAJUS 15 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 15 [hp_X]/mL
  • CROTALUS HORRIDUS HORRIDUS VENOM 15 [hp_X]/mL
  • DIGITALIS 15 [hp_X]/mL
  • EPINEPHRINE 15 [hp_X]/mL
  • GOLD 15 [hp_X]/mL
  • LACHESIS MUTA VENOM 15 [hp_X]/mL
  • MICRURUS CORALLINUS VENOM 30 [hp_X]/mL
  • NAJA NAJA VENOM 15 [hp_X]/mL
  • NITROGLYCERIN 15 [hp_X]/mL
  • POTASSIUM CARBONATE 15 [hp_X]/mL
  • POTASSIUM IODIDE 15 [hp_X]/mL
  • RUTA GRAVEOLENS FLOWERING TOP 6 [hp_X]/mL
  • SELENICEREUS GRANDIFLORUS STEM 15 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/mL
  • VALERIAN 6 [hp_X]/mL
  • VERATRUM ALBUM ROOT 15 [hp_X]/mL
  • VIPERA BERUS VENOM 16 [hp_X]/mL
  • VISCUM ALBUM FRUITING TOP 15 [hp_X]/mL
    • Pharmacologic Class(es):
  • Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
  • Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
  • Allergens - [CS]
  • Catecholamine - [EPC] (Established Pharmacologic Class)
  • Catecholamines - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Nitrate Vasodilator - [EPC] (Established Pharmacologic Class)
  • Nitrates - [CS]
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • Vasodilation - [PE] (Physiologic Effect)
  • alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
  • beta-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    05-09-2023
    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 55714-4848-1?

    The NDC Packaged Code 55714-4848-1 is assigned to a package of 30 ml in 1 bottle, glass of Hbp, a human over the counter drug labeled by Newton Laboratories, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 55714-4848 included in the NDC Directory?

    Yes, Hbp with product code 55714-4848 is active and included in the NDC Directory. The product was first marketed by Newton Laboratories, Inc. on May 09, 2023 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 55714-4848-1?

    The 11-digit format is 55714484801. 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
    5-4-155714-4848-15-4-255714-4848-01