Tap Water Detox Spray
NDC 83027-0093

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 83027-0093?
  4. Tap Water Detox Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Tap Water Detox (acetone, aluminium metallicum, antimonium crudum, arsenicum metallicum, baryta muriatica, cadmium metallicum, carbolicum acidum, chlorinum, chromium (metallicum), cuprum metallicum, ferrum metallicum, germanium metallicum, natrum fluoratum, plumbum metallicum, radium bromatum, vanadium metallicum, glyphosate herbicide) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Nutritional Specialties, 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 83027-0093 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
83027-0093
Proprietary Name:
Tap Water Detox
Non-Proprietary Name: [1]
Acetone, Aluminium Metallicum, Antimonium Crudum, Arsenicum Metallicum, Baryta Muriatica, Cadmium Metallicum, Carbolicum Acidum, Chlorinum, Chromium (metallicum), Cuprum Metallicum, Ferrum Metallicum, Germanium Metallicum, Natrum Fluoratum, Plumbum Metallicum, Radium Bromatum, Vanadium Metallicum, Glyphosate Herbicide
Substance Name: [2]
Acetone; Aluminum; Antimony Trisulfide; Arsenic; Barium Chloride Dihydrate; Cadmium; Chlorine; Chromium; Copper; Germanium; Glyphosate; Iron; Lead; Phenol; Radium Bromide; Sodium Fluoride; Vanadium
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]
Nutritional Specialties, Inc.
Labeler Code:
83027
Product Label ID:
37a48fea-a8df-4d27-b0c7-e5704c25e72f
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
07-11-2023
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 83027-0093?

The NDC code 83027-0093 is assigned by the FDA to the product Tap Water Detox. It is commonly known by its generic name, acetone, aluminium metallicum, antimonium crudum, arsenicum metallicum, baryta muriatica, cadmium metallicum, carbolicum acidum, chlorinum, chromium (metallicum), cuprum metallicum, ferrum metallicum, germanium metallicum, natrum fluoratum, plumbum metallicum, radium bromatum, vanadium metallicum, glyphosate herbicide. This pharmaceutical product is labeled by Nutritional Specialties, 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: 83027-0093-1. 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?

Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

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.
  • ACETONE 30 [hp_X]/mL - A colorless liquid used as a solvent and an antiseptic. It is one of the ketone bodies produced during ketoacidosis.
  • ALUMINUM 30 [hp_X]/mL - A metallic element that has the atomic number 13, atomic symbol Al, and atomic weight 26.98.
  • ANTIMONY TRISULFIDE 30 [hp_X]/mL - structure given in first source
  • ARSENIC 30 [hp_X]/mL - A shiny gray element with atomic symbol As, atomic number 33, and atomic weight 75. It occurs throughout the universe, mostly in the form of metallic arsenides. Most forms are toxic. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), arsenic and certain arsenic compounds have been listed as known carcinogens. (From Merck Index, 11th ed)
  • BARIUM CHLORIDE DIHYDRATE 30 [hp_X]/mL
  • CADMIUM 30 [hp_X]/mL - An element with atomic symbol Cd, atomic number 48, and atomic weight 112.41. It is a metal and ingestion will lead to CADMIUM POISONING.
  • CHLORINE 30 [hp_X]/mL - An element with atomic symbol Cl, atomic number 17, and atomic weight 35, and member of the halogen family.
  • CHROMIUM 30 [hp_X]/mL - A trace element that plays a role in glucose metabolism. It has the atomic symbol Cr, atomic number 24, and atomic weight 52. According to the Fourth Annual Report on Carcinogens (NTP85-002,1985), chromium and some of its compounds have been listed as known carcinogens.
  • COPPER 30 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
  • GERMANIUM 30 [hp_X]/mL - A rare metal element with a blue-gray appearance and atomic symbol Ge, atomic number 32, and atomic weight 72.63.
  • GLYPHOSATE 30 [hp_C]/mL - Active compound in herbicidal formulations that inhibits 3-PHOSPHOSHIKIMATE 1-CARBOXYVINYLTRANSFERASE.
  • IRON 30 [hp_X]/mL - A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.
  • LEAD 30 [hp_X]/mL - A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.
  • PHENOL 30 [hp_X]/mL - Benzene derivatives that include one or more hydroxyl groups attached to the ring structure.
  • RADIUM BROMIDE 30 [hp_X]/mL
  • SODIUM FLUORIDE 30 [hp_X]/mL - A source of inorganic fluoride which is used topically to prevent dental caries.
  • VANADIUM 30 [hp_X]/mL - A metallic element with the atomic symbol V, atomic number 23, and atomic weight 50.94. It is used in the manufacture of vanadium steel. Prolonged exposure can lead to chronic intoxication caused by absorption usually via the lungs.

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:

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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".