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NDC 50845-0249 Metals

Alumina,Aurum Metallicum,Carbo Vegetabilis,Causticum,Cysteinum,Hepar Suis,Hepar Sulphuris - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50845-0249?
  4. Metals Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 50845-0249 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
50845-0249
Proprietary Name:
Metals
Non-Proprietary Name: [1]
Alumina, Aurum Metallicum, Carbo Vegetabilis, Causticum, Cysteinum, Hepar Suis, Hepar Sulphuris Calcareum, Nitricum Acidum, Nux Vomica, Phytolacca Decandra, Platinum Metallicum, Stannum Metallicum, Stillingia Sylvatica, Tellurium Metallicum, X-ray
Substance Name: [2]
Activated Charcoal; Alcohol, X-ray Exposed (1000 Rad); Aluminum Oxide; Calcium Sulfide; Causticum; Cysteine; Gold; Nitric Acid; Phytolacca Americana Root; Platinum; Pork Liver; Stillingia Sylvatica Root; Strychnos Nux-vomica Seed; Tellurium; Tin
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
Liddell Laboratories, Inc.
Labeler Code:
50845
Product Label ID:
daa89e0d-1dd8-45eb-9f9b-0029fdcfecee
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
03-21-2019
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 50845-0249?

The NDC code 50845-0249 is assigned by the FDA to the product Metals which is a human over the counter drug product labeled by Liddell Laboratories, Inc.. The generic name of Metals is alumina, aurum metallicum, carbo vegetabilis, causticum, cysteinum, hepar suis, hepar sulphuris calcareum, nitricum acidum, nux vomica, phytolacca decandra, platinum metallicum, stannum metallicum, stillingia sylvatica, tellurium metallicum, x-ray. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 50845-0249-2 1 bottle, spray in 1 carton / 30 ml in 1 bottle, spray (50845-0249-1). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Metals?

Children 12 and under: Consult a doctor prior to use.Adults & children over 12: Spray twice under the tongue three times per day.For heavy exposure to toxic metals such as mercury, aluminum, and tin in dental amalgam fillings, or other toxic metals use daily for first month, then daily every other week. For light exposure, use daily the first month, then daily one week per month for the next three months.

What are Metals 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.
  • ACTIVATED CHARCOAL 12 [hp_X]/mL
  • ALCOHOL, X-RAY EXPOSED (1000 RAD) 30 [hp_C]/mL
  • ALUMINUM OXIDE 30 [hp_C]/mL - An oxide of aluminum, occurring in nature as various minerals such as bauxite, corundum, etc. It is used as an adsorbent, desiccating agent, and catalyst, and in the manufacture of dental cements and refractories.
  • CALCIUM SULFIDE 12 [hp_X]/mL
  • CAUSTICUM 12 [hp_X]/mL
  • CYSTEINE 12 [hp_X]/mL - A thiol-containing non-essential amino acid that is oxidized to form CYSTINE.
  • GOLD 30 [hp_C]/mL - A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.
  • NITRIC ACID 30 [hp_C]/mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
  • PHYTOLACCA AMERICANA ROOT 6 [hp_X]/mL
  • PLATINUM 30 [hp_C]/mL - A heavy, soft, whitish metal, resembling tin, with atomic number 78, atomic weight 195.084, symbol Pt. It is used in manufacturing equipment for laboratory and industrial use. It occurs as a black powder (platinum black) and as a spongy substance (spongy platinum) and may have been known in Pliny's time as alutiae.
  • PORK LIVER 6 [hp_X]/mL
  • STILLINGIA SYLVATICA ROOT 6 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • TELLURIUM 30 [hp_C]/mL - An element that is a member of the chalcogen family. It has the atomic symbol Te, atomic number 52, and atomic weight 127.60. It has been used as a coloring agent and in the manufacture of electrical equipment. Exposure may cause nausea, vomiting, and CNS depression.
  • TIN 30 [hp_C]/mL - A trace element that is required in bone formation. It has the atomic symbol Sn, atomic number 50, and atomic weight 118.71.

Which are Metals UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Metals 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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes for Metals?

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Product Footnotes

[1] 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.

[2] 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.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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] 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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".