Metals Spray
NDC 50845-0249

View dosage, usage, ingredients, routes, and UNII mappings.
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

Metals (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) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Liddell Laboratories, Inc.. This medication is typically used as a allergens [cs]. It is supplied as a spray for oral administration. This product entry covers the primary NDC 50845-0249 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

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
Code Navigator:

Clinical Specifications

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 & Regulatory Data

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.

Marketing Timeline

Start Marketing Date: [9]
03-21-2019
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 50845-0249?

The NDC code 50845-0249 is assigned by the FDA to the product Metals. It is commonly known by its generic name, 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. This pharmaceutical product is labeled by Liddell Laboratories, Inc. and is currently categorized as listed product. The medication is a spray administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 50845-0249-2. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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 Active Ingredients of this product?

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 - RN given refers to parent cpd; see also record for lime sulfur (calcium polysulfide)
  • CAUSTICUM 12 [hp_X]/mL - contains calcium hydroxide & potassium bisulfite; Homeopathic drug
  • 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 the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 of this product?

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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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".