NDC 43742-1649 Lung Drainage
Kali Muriaticum,Carbo Vegetabilis,Lung (suis),Mycoplasma Pneumoniae,Bryonia - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43742-1649?
What are the uses for Lung Drainage?
What are Lung Drainage Active Ingredients?
- ACTIVATED CHARCOAL 8 [hp_X]/mL
- ANTIMONY ARSENATE 30 [hp_X]/mL
- BRYONIA ALBA ROOT 12 [hp_X]/mL
- CAMPHOR (NATURAL) 30 [hp_X]/mL
- CHELIDONIUM MAJUS WHOLE 30 [hp_X]/mL
- COPPER 30 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
- GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/mL
- HAEMOPHILUS INFLUENZAE TYPE B 16 [hp_X]/mL - A type of H. influenzae isolated most frequently from biotype I. Prior to vaccine availability, it was a leading cause of childhood meningitis.
- IPECAC 30 [hp_X]/mL - A syrup made from the dried rhizomes of two different species, CEPHAELIS ipecacuanha and C. acuminata. They contain EMETINE, cephaeline, psychotrine and other ISOQUINOLINES. Ipecac syrup is used widely as an emetic acting both locally on the gastric mucosa and centrally on the chemoreceptor trigger zone.
- MYCOPLASMA PNEUMONIAE 12 [hp_X]/mL - Short filamentous organism of the genus Mycoplasma, which binds firmly to the cells of the respiratory epithelium. It is one of the etiologic agents of non-viral primary atypical pneumonia in man.
- OXYGEN 16 [hp_X]/mL - An element with atomic symbol O, atomic number 8, and atomic weight [15.99903; 15.99977]. It is the most abundant element on earth and essential for respiration.
- PHOSPHORUS 30 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- POLYGALA SENEGA ROOT 30 [hp_X]/mL
- POTASSIUM CHLORIDE 6 [hp_X]/mL - A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
- PRATIA PURPURASCENS 30 [hp_X]/mL
- QUININE HYDROCHLORIDE 30 [hp_X]/mL - An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood.
- STREPTOCOCCUS PNEUMONIAE 16 [hp_X]/mL - A gram-positive organism found in the upper respiratory tract, inflammatory exudates, and various body fluids of normal and/or diseased humans and, rarely, domestic animals.
- SUS SCROFA LUNG 8 [hp_X]/mL
- TIN 30 [hp_X]/mL - A trace element that is required in bone formation. It has the atomic symbol Sn, atomic number 50, and atomic weight 118.71.
- VERATRUM VIRIDE ROOT 30 [hp_X]/mL
Which are Lung Drainage UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- SUS SCROFA LUNG (UNII: 7GL3G1COB3)
- SUS SCROFA LUNG (UNII: 7GL3G1COB3) (Active Moiety)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- HAEMOPHILUS INFLUENZAE TYPE B (UNII: F2TW0N64FI)
- HAEMOPHILUS INFLUENZAE TYPE B (UNII: F2TW0N64FI) (Active Moiety)
- STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2)
- STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2) (Active Moiety)
- OXYGEN (UNII: S88TT14065)
- OXYGEN (UNII: S88TT14065) (Active Moiety)
- ANTIMONY ARSENATE (UNII: WE3458XNFT)
- ARSENATE ION (UNII: G1DBI405OK) (Active Moiety)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- QUININE HYDROCHLORIDE (UNII: 711S8Y0T33)
- QUININE (UNII: A7V27PHC7A) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
- PRATIA PURPURASCENS (UNII: 901NKD188B)
- PRATIA PURPURASCENS (UNII: 901NKD188B) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF)
- POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- VERATRUM VIRIDE ROOT (UNII: 197B3Q7T5Q)
- VERATRUM VIRIDE ROOT (UNII: 197B3Q7T5Q) (Active Moiety)
Which are Lung Drainage 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Lung Drainage?
- Antimalarial - [EPC] (Established Pharmacologic Class)
- Copper - [CS]
- Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
- Decreased Embryonic Implantation - [PE] (Physiologic Effect)
- Decreased Sperm Motility - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
* Please review the disclaimer below.
[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.
[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".