NDC 43742-1414 Bp Reg

Allium Sativum, Adrenalinum, Arteria Suis, Cortisone Aceticum, Thyroidinum (suis), Vena Suis, Formalinum, Kali Chloricum, Alpha-lipoicum Acidum, Aurum Metallicum, Cactus Grandiflorus, Cholesterinum, Coumarinum, Ephedra Vulgaris, Glonoinum, Lachesis Mutus, Rauwolfia Serpentina, Strontium Carbonicum, Sulphur, Veratrum Album, Proteus (vulgaris)

NDC Product Code 43742-1414

NDC CODE: 43742-1414

Proprietary Name: Bp Reg 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.

Non-Proprietary Name: Allium Sativum, Adrenalinum, Arteria Suis, Cortisone Aceticum, Thyroidinum (suis), Vena Suis, Formalinum, Kali Chloricum, Alpha-lipoicum Acidum, Aurum Metallicum, Cactus Grandiflorus, Cholesterinum, Coumarinum, Ephedra Vulgaris, Glonoinum, Lachesis Mutus, Rauwolfia Serpentina, Strontium Carbonicum, Sulphur, Veratrum Album, Proteus (vulgaris) 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Drug uses not available
  • Cortisone is a corticosteroid hormone (glucocorticoid). It decreases your body's natural defensive response and reduces symptoms such as swelling and allergic-type reactions. This medication is used to treat conditions such as arthritis, blood/hormone/immune system disorders, allergic reactions, certain skin and eye conditions, breathing problems, and certain cancers.
  • This medication is used as an antiperspirant to treat feet that sweat or smell excessively. It is also used as a drying agent during wart treatment.
  • This medication is used to relieve chest pain (angina) in people that have a certain heart condition (coronary artery disease). It may also be used before physical activities (such as exercise, sexual activity) to help prevent chest pain. Nitroglycerin belongs to a class of drugs known as nitrates. Angina occurs when the heart muscle is not getting enough blood. This drug works by relaxing and widening blood vessels so blood can flow more easily to the heart.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1414-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bp Reg with NDC 43742-1414 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Bp Reg is allium sativum, adrenalinum, arteria suis, cortisone aceticum, thyroidinum (suis), vena suis, formalinum, kali chloricum, alpha-lipoicum acidum, aurum metallicum, cactus grandiflorus, cholesterinum, coumarinum, ephedra vulgaris, glonoinum, lachesis mutus, rauwolfia serpentina, strontium carbonicum, sulphur, veratrum album, proteus (vulgaris). The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, Inc.

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.

Product Type: Human Otc Drug 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.

Bp Reg Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • GARLIC 6 [hp_X]/mL
  • EPINEPHRINE 8 [hp_X]/mL
  • SUS SCROFA ARTERY 8 [hp_X]/mL
  • CORTISONE ACETATE 8 [hp_X]/mL
  • THYROID, PORCINE 8 [hp_X]/mL
  • SUS SCROFA VEIN 8 [hp_X]/mL
  • FORMALDEHYDE 9 [hp_X]/mL
  • POTASSIUM CHLORATE 9 [hp_X]/mL
  • THIOCTIC ACID 12 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • SELENICEREUS GRANDIFLORUS STEM 12 [hp_X]/mL
  • CHOLESTEROL 12 [hp_X]/mL
  • COUMARIN 12 [hp_X]/mL
  • EPHEDRA DISTACHYA FLOWERING TWIG 12 [hp_X]/mL
  • NITROGLYCERIN 12 [hp_X]/mL
  • LACHESIS MUTA VENOM 12 [hp_X]/mL
  • RAUWOLFIA SERPENTINA 12 [hp_X]/mL
  • STRONTIUM CARBONATE 12 [hp_X]/mL
  • SULFUR 12 [hp_X]/mL
  • VERATRUM ALBUM ROOT 12 [hp_X]/mL
  • PROTEUS VULGARIS 16 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

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.
  • 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.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 12-06-2018 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Bp Reg Product Label Images

Bp Reg Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Allium Sativum 6X, Adrenalinum 8X, 12X, 30X, Arteria Suis 8X, 12X, 30X, Cortisone Aceticum 8X, 12X, 30X, Thyroidinum (Suis) 8X, 12X, 30X, Vena Suis 8X, 12X, 30X, Formalinum 9X, Kali Chloricum 12X, alpha-Lipoicum Acidum 12X, Aurum Metallicum 12X, Cactus Grandiflorus 12X, Cholesterinum 12X, Coumarinum 12X, Ephedra Vulgaris 12X, Glonoinum 12X, Lachesis Mutus 12X, Rauwolfia Serpentina 12X, Strontium Carbonicum 12X, Sulphur 12X, Veratrum Album 12X, Proteus (Vulgaris) 16X, 30X.

Homeopathic Indications:

For the temporary relief of symptoms related to blood pressure, such as headache, fatigue, confusion, and sexual dysfunction.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of symptoms related to blood pressure, such as headache, fatigue, confusion, and sexual dysfunction.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

Directions:

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.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-1414-1HOMEOPATHICBP REG1 FL OZ (30 ml)

* Please review the disclaimer below.