NDC 43742-0862 Bladder Kidney Meridian Formula

Cinnamic Acid, Phloridzinum, Alpha-ketoglutaricum Acidum, Ascorbic Acid, Kidney (suis), Malicum Acidum, Nicotinamidum, Urinary Bladder (suis), Adrenocorticotrophin, Apis Mellifica, Argentum Nitricum, Berberis Vulgaris, Cantharis, Equisetum Arvense, Kali Bichromicum, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Phosphorus, Rhus Tox, Sepia, Terebinthina, Thuja Occidentalis, Dysentery Bacillus, Faecalis (alkaligenes), Proteus (vulgaris)

NDC Product Code 43742-0862

NDC Code: 43742-0862

Proprietary Name: Bladder Kidney Meridian Formula 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: Cinnamic Acid, Phloridzinum, Alpha-ketoglutaricum Acidum, Ascorbic Acid, Kidney (suis), Malicum Acidum, Nicotinamidum, Urinary Bladder (suis), Adrenocorticotrophin, Apis Mellifica, Argentum Nitricum, Berberis Vulgaris, Cantharis, Equisetum Arvense, Kali Bichromicum, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Phosphorus, Rhus Tox, Sepia, Terebinthina, Thuja Occidentalis, Dysentery Bacillus, Faecalis (alkaligenes), 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.

NDC 43742-0862-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bladder Kidney Meridian Formula with NDC 43742-0862 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Bladder Kidney Meridian Formula is cinnamic acid, phloridzinum, alpha-ketoglutaricum acidum, ascorbic acid, kidney (suis), malicum acidum, nicotinamidum, urinary bladder (suis), adrenocorticotrophin, apis mellifica, argentum nitricum, berberis vulgaris, cantharis, equisetum arvense, kali bichromicum, lycopodium clavatum, mercurius solubilis, natrum muriaticum, phosphorus, rhus tox, sepia, terebinthina, thuja occidentalis, dysentery bacillus, faecalis (alkaligenes), 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.

Bladder Kidney Meridian Formula 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.

  • CINNAMIC ACID 6 [hp_X]/mL
  • PHLORIZIN 6 [hp_X]/mL
  • OXOGLURIC ACID 6 [hp_C]/mL
  • ASCORBIC ACID 6 [hp_C]/mL
  • PORK KIDNEY 6 [hp_C]/mL
  • MALIC ACID 6 [hp_C]/mL
  • NIACINAMIDE 6 [hp_C]/mL
  • SUS SCROFA URINARY BLADDER 6 [hp_C]/mL
  • CORTICOTROPIN 8 [hp_C]/mL
  • APIS MELLIFERA 30 [hp_C]/mL
  • SILVER NITRATE 30 [hp_C]/mL
  • BERBERIS VULGARIS ROOT BARK 30 [hp_C]/mL
  • LYTTA VESICATORIA 30 [hp_C]/mL
  • EQUISETUM ARVENSE TOP 30 [hp_C]/mL
  • POTASSIUM DICHROMATE 30 [hp_C]/mL
  • LYCOPODIUM CLAVATUM SPORE 30 [hp_C]/mL
  • MERCURIUS SOLUBILIS 30 [hp_C]/mL
  • SODIUM CHLORIDE 30 [hp_C]/mL
  • PHOSPHORUS 30 [hp_C]/mL
  • TOXICODENDRON PUBESCENS LEAF 30 [hp_C]/mL
  • SEPIA OFFICINALIS JUICE 30 [hp_C]/mL
  • TURPENTINE OIL 30 [hp_C]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_C]/mL
  • SHIGELLA DYSENTERIAE 30 [hp_C]/mL
  • ALCALIGENES FAECALIS 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: 10-04-2016 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: 07-24-2022 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.

Bladder Kidney Meridian Formula Product Label Images

Bladder Kidney Meridian Formula 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:

Cinnamic Acid 6X, 8X, 10X, 30X, 200X, Phloridzinum 6X, 8X, 10X, 30X, 200X, Alpha-Ketoglutaricum Acidum 6C, 30C, Ascorbic Acid 6C, 30C, Kidney (Suis) 6C, 30C, Malicum Acidum 6C, 30C, Nicotinamidum 6C, 30C, Urinary Bladder (Suis) 6C, 30C, Adrenocorticotrophin 8C, 30C, Apis Mellifica 30X, Argentum Nitricum 30C, Berberis Vulgaris 30C, Cantharis 30C, Equisetum Arvense 30C, Kali Bichromicum 30, Lycopodium Clavatum 30C, Mercurius Solubilis 30C, Natrum Muriaticum 30C, Phosphorus 30C, Rhus Tox 30C, Sepia 30C, Terebinthina 30C, Thuja Occidentalis 30C, Dysentery Bacillus 30C, 200C, Faecalis (Alkaligenes) 30C, 200C, Proteus (Vulgaris) 30C, 200C.

Homeopathic Indications:

For the temporary relief of symptoms of functional disorders of the bladder or urinary frequency, including fluid retention and burning.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of symptoms of functional disorders of the bladder or urinary frequency, including fluid retention and burning.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

If pregnant or breast-feeding, or have any allergic reaction to trace minerals, or any chronic or recurring symptoms or illness, consult a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store at room temperature.Keep out of direct sunlight.

Keep Out Of Reach Of Children:

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

Directions:

Adults 3 to 10 drops under the tongue 3 times daily or as directed by your health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

DISTRIBUTED BY:Deseret Biologicals, Inc., Sandy, UT 84070800.827.9529       www.desbio.com

Package Label Display:

NAMBUDRIPAD'S ALLERGY ELIMINATION TECHNIQUESNAETNDC 43742-0862-1HOMEOPATHICBLADDER/KIDNEYMeridian FormulaNet Contents 1 FL OZ (30 ML)DESBIO

* Please review the disclaimer below.