NDC 43742-1284 Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Taraxacum Officinale, Trifolium Pratense, Formalinum, Germanium Sesquioxide, Phytolacca Decandra, Acetone, Ammonium Muriaticum, Benzinum, Propylene Glycol, Sodium Lauryl Sulfate, Sodium Tripolyphosphate, Terebinthina, Methanol, Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum, Rhamnus Frangula
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What is NDC 43742-1284?
What are Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Taraxacum Officinale, Trifolium Pratense, Formalinum, Germanium Sesquioxide, Phytolacca Decandra, Acetone, Ammonium Muriaticum, Benzinum, Propylene Glycol, Sodium Lauryl Sulfate, Sodium Tripolyphosphate, Terebinthina, Methanol, Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum, Rhamnus Frangula Active Ingredients?
- ACETONE 9 [hp_X]/mL - A colorless liquid used as a solvent and an antiseptic. It is one of the ketone bodies produced during ketoacidosis.
- AMMONIUM CHLORIDE 9 [hp_X]/mL - An acidifying agent that has expectorant and diuretic effects. Also used in etching and batteries and as a flux in electroplating.
- ARCTIUM LAPPA ROOT 6 [hp_X]/mL
- BENZENE 9 [hp_X]/mL - Toxic, volatile, flammable liquid hydrocarbon byproduct of coal distillation. It is used as an industrial solvent in paints, varnishes, lacquer thinners, gasoline, etc. Benzene causes central nervous system damage acutely and bone marrow damage chronically and is carcinogenic. It was formerly used as parasiticide.
- BERBERIS VULGARIS ROOT BARK 6 [hp_X]/mL
- CHELIDONIUM MAJUS WHOLE 6 [hp_X]/mL
- FORMALDEHYDE SOLUTION 6 [hp_X]/mL
- FRANGULA ALNUS BARK 12 [hp_X]/mL
- GERMANIUM SESQUIOXIDE 8 [hp_X]/mL
- GLYCYRRHIZA GLABRA 6 [hp_X]/mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
- IRIDIUM 12 [hp_X]/mL - A metallic element with the atomic symbol Ir, atomic number 77, and atomic weight 192.22.
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- METHYL ALCOHOL 9 [hp_X]/mL - A colorless, flammable liquid used in the manufacture of FORMALDEHYDE and ACETIC ACID, in chemical synthesis, antifreeze, and as a solvent. Ingestion of methanol is toxic and may cause blindness.
- MILK THISTLE 6 [hp_X]/mL
- NITRIC ACID 12 [hp_X]/mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
- PHOSPHORIC ACID 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 8 [hp_X]/mL
- PROPYLENE GLYCOL 9 [hp_X]/mL - A clear, colorless, viscous organic solvent and diluent used in pharmaceutical preparations.
- SODIUM LAURYL SULFATE 9 [hp_X]/mL
- SODIUM TRIPOLYPHOSPHATE 9 [hp_X]/mL
- STILLINGIA SYLVATICA ROOT 6 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
- TARAXACUM OFFICINALE 6 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
- TRIFOLIUM PRATENSE FLOWER 6 [hp_X]/mL
- TURPENTINE OIL 9 [hp_X]/mL
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[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.
[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.
[10] 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.
[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".
[13] What is an Unfinished Product? - This field indicates if the product is an unfinished drug. An unfinished drug is an active pharmaceutical ingredient either alone or with other ingredients that is not a finished drug product. Unfinished drugs are used to process other drugs or for drug compounding.