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  5. NDC Package Code: 55714-2471-1 Jet Lag

NDC Package 55714-2471-1 Jet Lag

Echinacea,Alumina,Aralia Quinquefolia,Argentum,Arnica Montana,Arsenicum Album,Baptisia - 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:
55714-2471-1
Package Description:
30 mL in 1 BOTTLE, GLASS
Product Code:
55714-2471
Proprietary Name:
Jet Lag
Non-Proprietary Name:
Echinacea, Alumina, Aralia Quinquefolia, Argentum, Arnica Montana, Arsenicum Album, Baptisia Tinctoria, Bryonia, Cantharis, Chelidonium Majus, Conium Maculatum, Gelsemium Sempervirens, Iodium, Kali Carbonicum, Kali Iodatum, Lycopodium Clavatum, Lycopus Virginicus, Natrum Muriaticum, Nux Vomica, Phosphorus, Phytolacca Decandra, Pulsatilla, Rhus Toxicodendron, Sabal Serrulata, Thyroidinum.
Substance Name:
Aluminum Oxide; American Ginseng; Anemone Pulsatilla; Arnica Montana; Arsenic Trioxide; Baptisia Tinctoria Root; Bryonia Alba Root; Chelidonium Majus; Conium Maculatum Flowering Top; Echinacea, Unspecified; Gelsemium Sempervirens Root; Iodine; Lycopodium Clavatum Spore; Lycopus Virginicus; Lytta Vesicatoria; Phosphorus; Phytolacca Americana Root; Potassium Carbonate; Potassium Iodide; Saw Palmetto; Silver Nitrate; Sodium Chloride; Strychnos Nux-vomica Seed; Thyroid, Unspecified; Toxicodendron Pubescens Leaf
Usage Information:
Formulated for symptoms associated with travel and time change such as fatigue, sleeplessness, headaches, vomiting, cramping and other related symptoms.
11-Digit NDC Billing Format:
55714247101
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):
  • ALUMINUM OXIDE 15 [hp_X]/mL
  • AMERICAN GINSENG 15 [hp_X]/mL
  • ANEMONE PULSATILLA 15 [hp_X]/mL
  • ARNICA MONTANA 15 [hp_X]/mL
  • ARSENIC TRIOXIDE 15 [hp_X]/mL
  • BAPTISIA TINCTORIA ROOT 15 [hp_X]/mL
  • BRYONIA ALBA ROOT 15 [hp_X]/mL
  • CHELIDONIUM MAJUS 15 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 15 [hp_X]/mL
  • ECHINACEA, UNSPECIFIED 6 [hp_X]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 15 [hp_X]/mL
  • IODINE 15 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 15 [hp_X]/mL
  • LYCOPUS VIRGINICUS 15 [hp_X]/mL
  • LYTTA VESICATORIA 15 [hp_X]/mL
  • PHOSPHORUS 15 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 15 [hp_X]/mL
  • POTASSIUM CARBONATE 15 [hp_X]/mL
  • POTASSIUM IODIDE 15 [hp_X]/mL
  • SAW PALMETTO 15 [hp_X]/mL
  • SILVER NITRATE 15 [hp_X]/mL
  • SODIUM CHLORIDE 15 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/mL
  • THYROID, UNSPECIFIED 15 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 15 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    01-01-2019
    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 55714-2471-1?

    The NDC Packaged Code 55714-2471-1 is assigned to a package of 30 ml in 1 bottle, glass of Jet Lag, 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 55714-2471 included in the NDC Directory?

    Yes, Jet Lag with product code 55714-2471 is active and included in the NDC Directory. The product was first marketed by Newton Laboratories, Inc. on January 01, 2019 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 55714-2471-1?

    The 11-digit format is 55714247101. 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
    5-4-155714-2471-15-4-255714-2471-01