NDC 43742-0787 Metab

Ascorbicum Acidum, Cysteinum, Manganese Gluconate, Alpha-ketoglutaricum Acidum, Fumaricum Acidum, Germanium Sesquioxide, Iodium, Magnesium Metallicum, Natrum Oxalaceticum, Pulsatilla (vulgaris), Thyroidinum (suis), Vanadium Metallicum

NDC Product Code 43742-0787

NDC CODE: 43742-0787

Proprietary Name: Metab 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: Ascorbicum Acidum, Cysteinum, Manganese Gluconate, Alpha-ketoglutaricum Acidum, Fumaricum Acidum, Germanium Sesquioxide, Iodium, Magnesium Metallicum, Natrum Oxalaceticum, Pulsatilla (vulgaris), Thyroidinum (suis), Vanadium Metallicum 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
  • This medication is a mineral supplement used to prevent and treat low amounts of magnesium in the blood. Some brands are also used to treat symptoms of too much stomach acid such as stomach upset, heartburn, and acid indigestion. Magnesium is very important for the normal functioning of cells, nerves, muscles, bones, and the heart. Usually, a well-balanced diet provides normal blood levels of magnesium. However, certain situations cause your body to lose magnesium faster than you can replace it from your diet. These situations include treatment with water pills (diuretics such as furosemide, hydrochlorothiazide), a poor diet, alcoholism, or other medical conditions (e.g., severe diarrhea/vomiting, stomach/intestinal absorption problems, poorly controlled diabetes).

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc

NDC 43742-0787-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Metab with NDC 43742-0787 is a a human over the counter drug product labeled by Deseret Biologicals, Inc. The generic name of Metab is ascorbicum acidum, cysteinum, manganese gluconate, alpha-ketoglutaricum acidum, fumaricum acidum, germanium sesquioxide, iodium, magnesium metallicum, natrum oxalaceticum, pulsatilla (vulgaris), thyroidinum (suis), vanadium metallicum. 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.

Metab 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.

  • ASCORBIC ACID 6 [hp_X]/mL
  • CYSTEINE 9 [hp_X]/mL
  • MANGANESE GLUCONATE 10 [hp_X]/mL
  • OXOGLURIC ACID 12 [hp_X]/mL
  • FUMARIC ACID 12 [hp_X]/mL
  • GERMANIUM SESQUIOXIDE 12 [hp_X]/mL
  • IODINE 12 [hp_X]/mL
  • MAGNESIUM 12 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 12 [hp_X]/mL
  • ANEMONE PULSATILLA 12 [hp_X]/mL
  • SUS SCROFA THYROID 12 [hp_X]/mL
  • VANADIUM 12 [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: 06-27-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

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.

Metab Product Label Images

Metab 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:

Ascorbic Acid 6X, Cysteinum 9X, Manganese Gluconate 10X, Alpha-Ketoglutaricum Acidum 12X, Fumaricum Acidum 12X, Germanium Sesquioxide 12X, Iodium 12X, Magnesium Metallicum 12X, Natrum Oxalaceticum 12X, Pulsatilla (Vulgaris) 12X, Thyroidinum (Suis) 12X, Vanadium Metallicum 12X.

Homeopathic Indications:

For the temporary relief of symptoms related to headache, joint pain, sweating, congestion, and fatigue.****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 related to headache, joint pain, sweating, congestion, and fatigue.****These statements are based upon traditional 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 of breast-feeding, seek advice of 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 43742-0787-1HOMEOPATHICMETAB1 FL OZ (30 ml)

* Please review the disclaimer below.