| PRODUCT NDC | 72190-0001 | The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| PRODUCT TYPE NAME | HUMAN OTC DRUG | 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. |
| PROPRIETARY NAME | Metalock | 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 | Passiflora Incarnata, Chamomilla, Valeriana Officinalis, Fucus Officinalis, Agnus Castus, Kali Phosphoricum, Natrum Muriaticum, Nux Vomica, Phytolacca Decandra, Chelidonium Majus, Lycopodium Clavatum, Pituitarum Posterium (Bovine), Adrenocorticotrophin, Thyroidinum (Bovine), Thyroidinum (Ovine), Calcarea Carbonica, Carbo Vegetabilis, Magnesia Phosphorica, Natrum Phosphoricum, Ubidecarenonum, Graphites, Hypophysis Suis, Hypothalamus (Bovine), Placenta Totalis Suis, Argentum Nitricum, Berberis Vulgaris, | The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product. |
| DOSAGE FORM NAME | LIQUID | The translation of the dosage form Code submitted by the firm. |
| ROUTE NAME | ORAL | The translation of the route code submitted by the firm, indicating route of administration. |
| START MARKETING DATE | 4/4/2019 | This is the date that the labeler indicates was the start of its marketing of the drug product. |
| END MARKETING DATE | 4/18/2024 | 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. |
| MARKETING CATEGORY NAME | UNAPPROVED HOMEOPATHIC | 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. |
| LABELER NAME | Real Health Medical, LLC | Name of Company corresponding to the labeler code segment of the Product NDC. |
| SUBSTANCE NAME | ACTIVATED CHARCOAL; AESCULUS HIPPOCASTANUM FLOWER; AGRIMONIA EUPATORIA FLOWER; ANEMONE PULSATILLA; BERBERIS VULGARIS ROOT BARK; BOS TAURUS HYPOTHALAMUS; BOS TAURUS PITUITARY GLAND, POSTERIOR; BRYONIA ALBA ROOT; CASTANEA SATIVA LEAF; CENTAURIUM ERYTHRAEA FLOWER; CERATOSTIGMA WILLMOTTIANUM FLOWER; CHASTE TREE FRUIT; CHELIDONIUM MAJUS; CORTICOTROPIN; DATURA STRAMONIUM; DIBASIC POTASSIUM PHOSPHATE; DIGITALIS; FUCUS VESICULOSUS; GRAPHITE; IRIS VERSICOLOR ROOT; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MATRICARIA CHAMOMILLA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PASSIFLORA INCARNATA FLOWERING TOP; PHYTOLACCA AMERICANA ROOT; POTASSIUM CARBONATE; SCUTELLARIA LATERIFLORA; SEMECARPUS ANACARDIUM JUICE; SEPIA OFFICINALIS JUICE; SILVER NITRATE; SODIUM CARBONATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA PITUITARY GLAND; SUS SCROFA PLACENTA; THYROID, BOVINE; THYROID, OVINE; TOXICODENDRON PUBESCENS LEAF; UBIDECARENONE; VALERIAN | 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. |
| ACTIVE NUMERATOR STRENGTH | 12; 9; 6; 20; 20; 12; 10; 20; 6; 9; 6; 6; 6; 10; 20; 6; 20; 4; 12; 20; 6; 12; 3; 12; 3; 6; 20; 20; 200; 20; 20; 20; 6; 12; 20; 6; 12; 12; 10; 1; 20; 12; 3 | |
| ACTIVE INGRED UNIT | [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_Q]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL | |
| PHARM CLASSES | Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] | |