NDC 37662-2730 Aurum Muriaticum Natronatum
Pellet Oral

Product Information

What is NDC 37662-2730?

The NDC code 37662-2730 is assigned by the FDA to the product Aurum Muriaticum Natronatum which is a human over the counter drug product labeled by Hahnemann Laboratories, Inc.. The product's dosage form is pellet and is administered via oral form. The product is distributed in 4 packages with assigned NDC codes 37662-2730-1 200 pellet in 1 vial, glass , 37662-2730-2 500 pellet in 1 vial, glass , 37662-2730-3 3000 pellet in 1 bottle, glass , 37662-2730-4 10000 pellet in 1 bottle, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code37662-2730
Proprietary Name 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.		Aurum Muriaticum Natronatum
Non-Proprietary Name 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.		Aurum Muriaticum Natronatum
Substance Name What is the Substance Name?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.		Sodium Tetrachloroaurate
Product Type 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.		Human Otc Drug
Dosage FormPellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Hahnemann Laboratories, Inc.
Labeler Code37662
Marketing Category 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.		UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		02-28-2023
Listing Expiration Date What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.		12-31-2024
Exclude Flag 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". 		N
NDC Code Structure

Product Characteristics

Color(s)WHITE (C48325)
ShapeROUND (C48348)
Size(s)3 MM
2 MM
Score1

Product Packages

NDC Code 37662-2730-1

Package Description: 200 PELLET in 1 VIAL, GLASS

NDC Code 37662-2730-2

Package Description: 500 PELLET in 1 VIAL, GLASS

NDC Code 37662-2730-3

Package Description: 3000 PELLET in 1 BOTTLE, GLASS

NDC Code 37662-2730-4

Package Description: 10000 PELLET in 1 BOTTLE, GLASS

Product Details

What are Aurum Muriaticum Natronatum Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Aurum Muriaticum Natronatum Active Ingredients UNII Codes

  • SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299)
  • TETRACHLOROAURATE ION (UNII: ZNL6IP5PJX) (Active Moiety)

Aurum Muriaticum Natronatum Inactive Ingredients UNII Codes

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

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Aurum Muriaticum Natronatum Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



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