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  5. NDC Package Code: 71144-0001-1 Cold And Flu Relief

NDC Package 71144-0001-1 Cold And Flu Relief

Baptisia Tinctoria,Calcarea Sulphurica,Allium Cepa,Calcarea Carbonica,Calcarea - 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:
71144-0001-1
Package Description:
60 mL in 1 BOTTLE, SPRAY
Product Code:
71144-0001
Proprietary Name:
Cold And Flu Relief
Non-Proprietary Name:
Baptisia Tinctoria, Calcarea Sulphurica, Allium Cepa, Calcarea Carbonica, Calcarea Phosphorica, Ferrum Phosphoricum, Kali Muriaticum, Kali Sulphuricum, Silicea, Spongia Tosta, Aconitum Napellus, Arsenicum Album, Dulcamara, Euphrasia Officinalis, Eupatorium Perfoliatum, Gelsemium Sempervirens
Substance Name:
Aconitum Napellus; Arsenic Trioxide; Baptisia Tinctoria Root; Calcium Sulfate Anhydrous; Eupatorium Perfoliatum Flowering Top; Euphrasia Stricta; Ferrum Phosphoricum; Gelsemium Sempervirens Root; Onion; Oyster Shell Calcium Carbonate, Crude; Potassium Chloride; Potassium Sulfate; Silicon Dioxide; Solanum Dulcamara Top; Spongia Officinalis Skeleton, Roasted; Tribasic Calcium Phosphate
Usage Information:
For temporary relief of cold and flu symptoms, such as sinus congestion, achiness, chills, headache, sore throat and fever.  For best results use at the first sign of a cold or flu. For temporary relief of cold and flu symptoms, such as sinus congestion, achiness, chills, headache, sore throat and fever. For best results use at the first sign of a cold or flu.
11-Digit NDC Billing Format:
71144000101
Product Type:
Human Otc Drug
Labeler Name:
Attuned Matrix, Llc
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACONITUM NAPELLUS 12 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
  • CALCIUM SULFATE ANHYDROUS 6 [hp_X]/mL
  • EUPATORIUM PERFOLIATUM FLOWERING TOP 12 [hp_X]/mL
  • EUPHRASIA STRICTA 12 [hp_X]/mL
  • FERRUM PHOSPHORICUM 8 [hp_X]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/mL
  • ONION 8 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL
  • POTASSIUM CHLORIDE 8 [hp_X]/mL
  • POTASSIUM SULFATE 8 [hp_X]/mL
  • SILICON DIOXIDE 8 [hp_X]/mL
  • SOLANUM DULCAMARA TOP 12 [hp_X]/mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED 8 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 8 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Cations, Divalent - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Potassium Compounds - [CS]
  • Potassium Salt - [EPC] (Established Pharmacologic Class)
  • Vegetable Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    01-19-2017
    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 71144-0001-1?

    The NDC Packaged Code 71144-0001-1 is assigned to a package of 60 ml in 1 bottle, spray of Cold And Flu Relief, a human over the counter drug labeled by Attuned Matrix, Llc. The product's dosage form is spray and is administered via oral form.

    Is NDC 71144-0001 included in the NDC Directory?

    Yes, Cold And Flu Relief with product code 71144-0001 is active and included in the NDC Directory. The product was first marketed by Attuned Matrix, Llc on January 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 71144-0001-1?

    The 11-digit format is 71144000101. 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
    5-4-171144-0001-15-4-271144-0001-01