NDC 43742-1034 Pericardium/triple Warmer Meridian Formula

Norepinephrine, Octopamine (hydrochloride), Insulinum (suis), Hydrocortisone (cortisol), Ascorbic Acid, Glandula Suprarenalis Suis, Heart (suis), Hypophysis Suis, Sarcolacticum Acidum, Thyroidinum (suis), Adrenocorticotrophin, Gaertner Bacillus (bach), Ubidecarenonum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Calcarea Carbonica, Glonoinum, Iodium, Kali Iodatum, Lachesis Mutus, Lithium Carbonicum, Lobelia Inflata, Mercurius Solubilis, Naja Tripudians, Phosphoricum Acidum, Phosphorus, Sepia,

NDC Product Code 43742-1034

NDC CODE: 43742-1034

Proprietary Name: Pericardium/triple Warmer 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: Norepinephrine, Octopamine (hydrochloride), Insulinum (suis), Hydrocortisone (cortisol), Ascorbic Acid, Glandula Suprarenalis Suis, Heart (suis), Hypophysis Suis, Sarcolacticum Acidum, Thyroidinum (suis), Adrenocorticotrophin, Gaertner Bacillus (bach), Ubidecarenonum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Calcarea Carbonica, Glonoinum, Iodium, Kali Iodatum, Lachesis Mutus, Lithium Carbonicum, Lobelia Inflata, Mercurius Solubilis, Naja Tripudians, Phosphoricum Acidum, Phosphorus, Sepia, 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.

  • This medication is used to treat a variety of skin conditions (e.g., insect bites, poison oak/ivy, eczema, dermatitis, allergies, rash, itching of the outer female genitals, anal itching). Hydrocortisone reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a mild corticosteroid.
  • Drug uses not available
  • Drug uses not available
  • Coenzyme Q10 has been used for heart problems (e.g., heart failure, angina), high blood pressure, Parkinson's disease, gum disease, and certain diseases passed down through families (Huntington's disease, muscular dystrophy). It has also been used for reducing the number of migraine headaches and for reducing cell damage that may occur after surgery or treatment with certain anti-cancer drugs. If you have or think you have any of the conditions listed above, consult your doctor for advice on proper care and treatment. Coenzyme Q10 is a substance that your body normally makes. Your body uses it to help keep in good health. Some herbal/diet supplement products have been found to contain possibly harmful impurities/additives. Check with your pharmacist for more details about the brand you use. The FDA has not reviewed this product for safety or effectiveness. Consult your doctor or pharmacist for more details.
  • Arsenic trioxide is used to treat a type of leukemia (acute promyelocytic leukemia-APL).
  • 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.
  • Potassium iodide is used to loosen and break up mucus in the airways. This helps you cough up the mucus so you can breathe more easily if you have long-term lung problems (e.g., asthma, chronic bronchitis, emphysema). This medication is known as an expectorant. Potassium iodide is also used along with antithyroid medicines to prepare the thyroid gland for surgical removal, to treat certain overactive thyroid conditions (hyperthyroidism), and to protect the thyroid in a radiation exposure emergency. It works by shrinking the size of the thyroid gland and decreasing the amount of thyroid hormones produced. In a radiation emergency, potassium iodide blocks only the thyroid from absorbing radioactive iodine, protecting it from damage and reducing the risk of thyroid cancer. Use this medication along with other emergency measures that will be recommended to you by public health and safety officials (e.g., finding safe shelter, evacuation, controlling food supply).
  • This medication is used to treat manic-depressive disorder (bipolar disorder). It works to stabilize the mood and reduce extremes in behavior by restoring the balance of certain natural substances (neurotransmitters) in the brain. Some of the benefits of continued use of this medication include decreasing how often manic episodes occur and decreasing the symptoms of manic episodes, such as exaggerated feelings of well-being, feelings that others wish to harm you, irritability, anxiousness, rapid/loud speech, and aggressive/hostile behaviors.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.
    • 43742-1034 - Pericardium/triple Warmer Meridian Formula

NDC 43742-1034-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Pericardium/triple Warmer Meridian Formula with NDC 43742-1034 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Pericardium/triple Warmer Meridian Formula is norepinephrine, octopamine (hydrochloride), insulinum (suis), hydrocortisone (cortisol), ascorbic acid, glandula suprarenalis suis, heart (suis), hypophysis suis, sarcolacticum acidum, thyroidinum (suis), adrenocorticotrophin, gaertner bacillus (bach), ubidecarenonum, arsenicum album, aurum metallicum, baryta carbonica, calcarea carbonica, glonoinum, iodium, kali iodatum, lachesis mutus, lithium carbonicum, lobelia inflata, mercurius solubilis, naja tripudians, phosphoricum acidum, phosphorus, sepia, . 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.

Pericardium/triple Warmer 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.

  • NOREPINEPHRINE 6 [hp_X]/mL
  • OCTOPAMINE 6 [hp_X]/mL
  • INSULIN PORK 15 [hp_X]/mL
  • HYDROCORTISONE 6 [hp_C]/mL
  • ASCORBIC ACID 6 [hp_C]/mL
  • SUS SCROFA ADRENAL GLAND 6 [hp_C]/mL
  • PORK HEART 6 [hp_C]/mL
  • SUS SCROFA PITUITARY GLAND 6 [hp_C]/mL
  • LACTIC ACID, L- 6 [hp_C]/mL
  • SUS SCROFA THYROID 6 [hp_C]/mL
  • CORTICOTROPIN 8 [hp_C]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 8 [hp_C]/mL
  • UBIDECARENONE 8 [hp_C]/mL
  • ARSENIC TRIOXIDE 30 [hp_C]/mL
  • GOLD 30 [hp_C]/mL
  • BARIUM CARBONATE 30 [hp_C]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL
  • NITROGLYCERIN 30 [hp_C]/mL
  • IODINE 30 [hp_C]/mL
  • POTASSIUM IODIDE 30 [hp_C]/mL
  • LACHESIS MUTA VENOM 30 [hp_C]/mL
  • LITHIUM CARBONATE 30 [hp_C]/mL
  • LOBELIA INFLATA 30 [hp_C]/mL
  • MERCURIUS SOLUBILIS 30 [hp_C]/mL
  • NAJA NAJA VENOM 30 [hp_C]/mL
  • PHOSPHORIC ACID 30 [hp_C]/mL
  • PHOSPHORUS 30 [hp_C]/mL
  • SEPIA OFFICINALIS JUICE 30 [hp_C]/mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED 30 [hp_C]/mL
  • PROTEUS MORGANII 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.
  • 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: 01-02-2018 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 08-04-2022 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.

Pericardium/triple Warmer Meridian Formula Product Label Images

Pericardium/triple Warmer 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:

Norepinephrine 6X, 8X, 30X, 200X, Octopamine (Hydrochloride) 6X, 8X, 30X, 200X, Insulinum (Suis) 15X, 30X, 200X, Hydrocortisone (Cortisol) 6C, Ascorbic Acid 6C, 30C, Glandula Suprarenalis Suis 6C, 30C, Heart (Suis) 6C, 30C, Pituitaria Glandula 6C, 30C, Sarcolacticum Acidum 6C, 30C, Thyroidinum (Suis) 6C, 30C, Adrenocorticotrophin 8C, 30C, Gaertner Bacillus (Bach) 8C, 30C, Ubidecarenonum 8C, 30C, Arsenicum Album 30C, Aurum Metallicum 30C, Baryta Carbonica 30C, Calcarea Carbonica 30C, Glonoinum 30C, Iodium 30C, Kali Iodatum 30C, Lachesis Mutus 30C, Lithium Carbonicum 30C, Lobelia Inflata 30C, Mercurius Solubilis 30C, Naja Tripudians 30C, Phosphoricum Acidum 30C, Phosphorus 30C, Sepia 30C, Spongia Tosta 30C, Proteus (Morgani) 30C, 200C.

Indications:

Temporary relief of symptoms related to energy weakness in the circulation and endocrine symptoms including fatigue, nervousness, achiness and headaches.

Temporary relief of symptoms related to energy weakness in the circulation and endocrine symptoms including fatigue, nervousness, achiness and headaches.

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:

NAMIBUDRIPAD'S ALLERGY ELIMINATION TECHNIQUESNAETNDC 43742-1034-1HOMEOPATHICPERICARDIUM/TRIPLE WARMERMeridian FormulaNet Contents 1 FL OZ (30 ML)DESBIO

* Please review the disclaimer below.