Bp Reg Liquid
NDC 43742-2177

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-2177?
  4. Bp Reg Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Bp Reg (adrenalinum, allium sativum, alpha-lipoicum acidum, arteria suis, aurum metallicum, cactus grandiflorus, cholesterinum, cortisone aceticum, coumarinum, formalinum, glonoinum, kali chloricum, lachesis mutus, proteus (vulgaris), rauwolfia serpentina, strontium carbonicum, sulphur, thyroidinum (suis), vena suis, veratrum album) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a adrenergic alpha-agonists [moa]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-2177 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-2177
Proprietary Name:
Bp Reg
Non-Proprietary Name: [1]
Adrenalinum, Allium Sativum, Alpha-lipoicum Acidum, Arteria Suis, Aurum Metallicum, Cactus Grandiflorus, Cholesterinum, Cortisone Aceticum, Coumarinum, Formalinum, Glonoinum, Kali Chloricum, Lachesis Mutus, Proteus (vulgaris), Rauwolfia Serpentina, Strontium Carbonicum, Sulphur, Thyroidinum (suis), Vena Suis, Veratrum Album
Substance Name: [2]
Alpha Lipoic Acid; Cholesterol; Cortisone Acetate; Coumarin; Epinephrine; Formaldehyde Solution; Garlic; Gold; Lachesis Muta Venom; Nitroglycerin; Potassium Chlorate; Proteus Vulgaris; Rauwolfia Serpentina; Selenicereus Grandiflorus Stem; Strontium Carbonate; Sulfur; Sus Scrofa Artery; Sus Scrofa Vein; Thyroid; Veratrum Album Root
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Deseret Biologicals, Inc.
Labeler Code:
43742
Product Label ID:
540c1149-b6d4-4926-87e8-73a920f87b4a
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
05-09-2024
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-2177?

The NDC code 43742-2177 is assigned by the FDA to the product Bp Reg. It is commonly known by its generic name, adrenalinum, allium sativum, alpha-lipoicum acidum, arteria suis, aurum metallicum, cactus grandiflorus, cholesterinum, cortisone aceticum, coumarinum, formalinum, glonoinum, kali chloricum, lachesis mutus, proteus (vulgaris), rauwolfia serpentina, strontium carbonicum, sulphur, thyroidinum (suis), vena suis, veratrum album. This pharmaceutical product is labeled by Deseret Biologicals, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43742-2177-1. 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?

1-10 drops under the tongue, 3 times a day or as directed by a health professional. 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.
  • ALPHA LIPOIC ACID 12 [hp_X]/mL - An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
  • CHOLESTEROL 12 [hp_X]/mL - The principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils.
  • CORTISONE ACETATE 8 [hp_X]/mL - A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726)
  • COUMARIN 12 [hp_X]/mL - Synthetic or naturally occurring substances related to coumarin, the delta-lactone of coumarinic acid.
  • EPINEPHRINE 8 [hp_X]/mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
  • FORMALDEHYDE SOLUTION 9 [hp_X]/mL
  • GARLIC 6 [hp_X]/mL - A species of Allium used as a spice (SPICES) and traditional remedy. It contains alliin lyase and alliin, which is converted by alliin lyase to allicin, the pungent ingredient responsible for the aroma of fresh cut garlic.
  • GOLD 12 [hp_X]/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.
  • LACHESIS MUTA VENOM 12 [hp_X]/mL
  • NITROGLYCERIN 12 [hp_X]/mL - A volatile vasodilator which relieves ANGINA PECTORIS by stimulating GUANYLATE CYCLASE and lowering cytosolic calcium. It is also sometimes used for TOCOLYSIS and explosives.
  • POTASSIUM CHLORATE 9 [hp_X]/mL
  • PROTEUS VULGARIS 16 [hp_X]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that occurs in soil, fecal matter, and sewage. It is an opportunistic pathogen and causes cystitis and pyelonephritis.
  • RAUWOLFIA SERPENTINA 12 [hp_X]/mL - A plant genus of the APOCYNACEAE or dogbane family. Alkaloids from plants in this genus have been used as tranquilizers and antihypertensive agents. RESERPINE is derived from R. serpentina.
  • SELENICEREUS GRANDIFLORUS STEM 12 [hp_X]/mL
  • STRONTIUM CARBONATE 12 [hp_X]/mL
  • SULFUR 12 [hp_X]/mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
  • SUS SCROFA ARTERY 8 [hp_X]/mL
  • SUS SCROFA VEIN 8 [hp_X]/mL
  • THYROID 8 [hp_X]/mL - A highly vascularized endocrine gland consisting of two lobes joined by a thin band of tissue with one lobe on each side of the TRACHEA. It secretes THYROID HORMONES from the follicular cells and CALCITONIN from the parafollicular cells thereby regulating METABOLISM and CALCIUM level in blood, respectively.
  • VERATRUM ALBUM ROOT 12 [hp_X]/mL

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?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients 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".