NDC 44911-0401-1 Throatspray

Echinacea (angustifolia), Eugenia Caryophyllata, Glycerinum, Myrrha, Salvia Officinalis, Spilanthes Oleracea, Thymus Serpyllum, Baptisia Tinctoria, Phytolacca Decandra, Hydrastis Canadensis, Apis Mellifica, Belladonna, Lachesis Mutus, Mercurius Solubilis, Hepar Sulphuris Calcareum

NDC Package Code 44911-0401-1

The NDC Code 44911-0401-1 is assigned to a package of 60 ml in 1 bottle, spray of Throatspray, a human over the counter drug labeled by Energique, Inc.. The product's dosage form is spray and is administered via oral form.

Field Name Field Value
NDC Code 44911-0401-1
Package Description 60 mL in 1 BOTTLE, SPRAY
Proprietary Name Throatspray What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Echinacea (angustifolia), Eugenia Caryophyllata, Glycerinum, Myrrha, Salvia Officinalis, Spilanthes Oleracea, Thymus Serpyllum, Baptisia Tinctoria, Phytolacca Decandra, Hydrastis Canadensis, Apis Mellifica, Belladonna, Lachesis Mutus, Mercurius Solubilis, Hepar Sulphuris Calcareum What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
11-Digit NDC Billing Format 44911040101 NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
Product Type Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Labeler Name Energique, Inc.
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)
  • ECHINACEA ANGUSTIFOLIA 1 [hp_X]/mL
  • CLOVE 1 [hp_X]/mL
  • GLYCERIN 1 [hp_X]/mL
  • MYRRH 2 [hp_X]/mL
  • SAGE 2 [hp_X]/mL
  • ACMELLA OLERACEA FLOWERING TOP 2 [hp_X]/mL
  • THYMUS SERPYLLUM 2 [hp_X]/mL
  • BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL
  • GOLDENSEAL 6 [hp_X]/mL
  • APIS MELLIFERA 12 [hp_X]/mL
  • ATROPA BELLADONNA 12 [hp_X]/mL
  • LACHESIS MUTA VENOM 12 [hp_X]/mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/mL
  • CALCIUM SULFIDE 15 [hp_X]/mL
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Marketing Category UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date 10-13-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
End Marketing Date 12-30-2021 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Exclude Flag N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

NDC Code Structure

  • 44911 - Energique, Inc.
    • 44911-0401 - Throatspray
      • 44911-0401-1 - 60 mL in 1 BOTTLE, SPRAY

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.

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