NDC 83027-0116 Metab

Calcarea Sulphurica,Kali Muriaticum,Kali Phosphoricum,Kali Sulphuricum,Natrum - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
Proprietary Name:
Non-Proprietary Name: [1]
Calcarea Sulphurica, Kali Muriaticum, Kali Phosphoricum, Kali Sulphuricum, Natrum Muriaticum, Natrum Phosphoricum, Natrum Sulphuricum, Cerebellum (suis), Gallbladder (bovine), Heart (bovine), Hepar (bovine), Hypothalamus Suis, Intestine (suis), Kidney (bovine), Lung (bovine), Medulla Ossis Suis, Pancreas Suis, Pineal Gland (suis), Rectal Mucosa (suis), Spleen (bovine), Stomach (suis), Thymus (ovine), Thyroidinum (bovine), Urinary Bladder (suis), Pituitarum Posterium (bovine), Acetyl Coenzyme A,
Substance Name: [2]
Acetyl Coenzyme A; Aconitic Acid; Alanine; Anhydrous Citric Acid; Arginine; Asparagine; Aspartic Acid; Beef Heart; Beef Kidney; Beef Liver; Beef Lung; Bos Taurus Gallbladder; Bos Taurus Parathyroid Gland; Bos Taurus Pituitary Gland, Posterior; Bos Taurus Spleen; Calcium Fluoride; Calcium Sulfate Anhydrous; Cysteine; Dibasic Potassium Phosphate; Ferrosoferric Phosphate; Fumaric Acid; Glutamic Acid; Glutamine; Glycine; Herring Sperm Dna; Histidine; Isoleucine; Lamb; Leucine; Lysine; Magnesium Phosphate, Dibasic Trihydrate; Malic Acid; Methionine; Oxogluric Acid; Phenylalanine; Pork Intestine; Potassium Chloride; Potassium Sulfate; Proline; Saccharomyces Cerevisiae Rna; Serine; Silicon Dioxide; Sodium Chloride; Sodium Phosphate, Dibasic, Heptahydrate; Sodium Sulfate; Succinic Acid; Sus Scrofa Bone Marrow; Sus Scrofa Cerebellum; Sus Scrofa Hypothalamus; Sus Scrofa Pancreas; Sus Scrofa Pineal Gland; Sus Scrofa Rectal Mucosa; Sus Scrofa Stomach; Sus Scrofa Urinary Bladder; Threonine; Thyroid, Bovine; Tribasic Calcium Phosphate; Tyrosine; Valine
NDC Directory Status:
Human Otc Drug
Product Type: [3]
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Code:
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    Listing Expiration Date: [11]
    Exclude Flag: [12]
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    Product Details

    What is NDC 83027-0116?

    The NDC code 83027-0116 is assigned by the FDA to the product Metab which is a human over the counter drug product labeled by Nutritional Specialties, Inc.. The generic name of Metab is calcarea sulphurica, kali muriaticum, kali phosphoricum, kali sulphuricum, natrum muriaticum, natrum phosphoricum, natrum sulphuricum, cerebellum (suis), gallbladder (bovine), heart (bovine), hepar (bovine), hypothalamus suis, intestine (suis), kidney (bovine), lung (bovine), medulla ossis suis, pancreas suis, pineal gland (suis), rectal mucosa (suis), spleen (bovine), stomach (suis), thymus (ovine), thyroidinum (bovine), urinary bladder (suis), pituitarum posterium (bovine), acetyl coenzyme a, . The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 83027-0116-1 60 ml in 1 bottle, spray . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Metab?

    Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

    What are Metab Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Metab UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Metab Inactive Ingredients UNII Codes?

    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. The UNII codes for the inactive ingredients in this product are:

    Which are the Pharmacologic Classes for Metab?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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    Product Footnotes

    [1] 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.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] 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.

    [12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".