NDC 43742-0469 Prostate

Petroselinum Sativum, Populus Tremulodies, Sabal Serrulata, Chimaphila Umbellata, Adenosinum Triphosphoricum Dinatrum, Equol, Kreosotum, Nadidum, Testosterone, Succinicum Acidum, Hepar Sulphuris Calcareum, Prostate Nosode, Conium Maculatum, Proteus (mirabilis), Proteus (vulgaris)

NDC Product Code 43742-0469

NDC Code: 43742-0469

Proprietary Name: Prostate 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: Petroselinum Sativum, Populus Tremulodies, Sabal Serrulata, Chimaphila Umbellata, Adenosinum Triphosphoricum Dinatrum, Equol, Kreosotum, Nadidum, Testosterone, Succinicum Acidum, Hepar Sulphuris Calcareum, Prostate Nosode, Conium Maculatum, Proteus (mirabilis), 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.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.
    • 43742-0469 - Prostate

NDC 43742-0469-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Prostate with NDC 43742-0469 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Prostate is petroselinum sativum, populus tremulodies, sabal serrulata, chimaphila umbellata, adenosinum triphosphoricum dinatrum, equol, kreosotum, nadidum, testosterone, succinicum acidum, hepar sulphuris calcareum, prostate nosode, conium maculatum, proteus (mirabilis), 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.

Prostate 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.

  • PETROSELINUM CRISPUM 4 [hp_X]/mL
  • POPULUS TREMULOIDES BARK 4 [hp_X]/mL
  • POPULUS TREMULOIDES LEAF 4 [hp_X]/mL
  • SAW PALMETTO 4 [hp_X]/mL
  • CHIMAPHILA UMBELLATA 5 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 6 [hp_X]/mL
  • EQUOL, (+/-)- 6 [hp_X]/mL
  • WOOD CREOSOTE 6 [hp_X]/mL
  • NADIDE 6 [hp_X]/mL
  • TESTOSTERONE 6 [hp_X]/mL
  • SUCCINIC ACID 8 [hp_X]/mL
  • CALCIUM SULFIDE 10 [hp_X]/mL
  • SUS SCROFA PROSTATE 11 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 30 [hp_X]/mL
  • PROTEUS MIRABILIS 30 [hp_C]/mL
  • PROTEUS VULGARIS 30 [hp_C]/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.

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: 03-20-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 05-20-2020 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Prostate Product Label Images

Prostate 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:

Petroselinum Sativum 4X, Populus Tremuloides 4X, Sabal Serrulata 4X, Chimaphila Umbellata 5X, Adenosinum Triphosphoricum Dinatrum 6X, Equol 6X, Kreosotum 6X, Nadidum 6X, Testosterone 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Succinicum Acidum 8X, Hepar Sulphuris Calcareum 10X, Prostate Nosode 11X, Conium Maculatum 30X, Proteus (Mirabilis) 30C, Proteus (Vulgaris) 30C.

Indications:

For temporary relief of the symptoms of prostate issues including weak stream and frequent urination.

For temporary relief of the symptoms of prostate issues including weak stream and frequent urination.

Warnings:

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

Directions:

1-10 drops under the tongue, 2 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 Parkland DriveSandy, UT 84070    www.desbio.com

Package Label Display:

DESBIONDC 43742-0469-1HOMEOPATHICPROSTATE1 FL OZ (30 ml)

* Please review the disclaimer below.

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