NDC 62795-1022 Bhi Cough
Antimony Potassium Tartrate,Atropa Belladonna,Blatta Orientalis,Bryonia Alba Whole,Anemone - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 62795-1022?
What are the uses for Bhi Cough?
What are Bhi Cough Active Ingredients?
- ANEMONE HEPATICA VAR. OBTUSA 5 [hp_X]/1
- ANTIMONY POTASSIUM TARTRATE 6 [hp_X]/1 - A schistosomicide possibly useful against other parasites. It has irritant emetic properties and may cause lethal cardiac toxicity among other adverse effects.
- ASPIDOSPERMA QUEBRACHO-BLANCO BARK 6 [hp_X]/1
- ATROPA BELLADONNA 6 [hp_X]/1 - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
- BLATTA ORIENTALIS 8 [hp_X]/1
- BRYONIA ALBA WHOLE 8 [hp_X]/1
- IPECAC 4 [hp_X]/1 - 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.
- LOBELIA INFLATA 5 [hp_X]/1 - A plant genus of the family CAMPANULACEAE used medicinally and is a source of LOBELINE.
- NAPHTHALENE 6 [hp_X]/1
- SODIUM SULFIDE NONAHYDRATE 6 [hp_X]/1
- STACHYS OFFICINALIS 4 [hp_X]/1
- STAR ANISE 4 [hp_X]/1
Which are Bhi Cough UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
- ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- BLATTA ORIENTALIS (UNII: 535787266D)
- BLATTA ORIENTALIS (UNII: 535787266D) (Active Moiety)
- BRYONIA ALBA WHOLE (UNII: 56K0VVT47P)
- BRYONIA ALBA WHOLE (UNII: 56K0VVT47P) (Active Moiety)
- ANEMONE AMERICANA (UNII: 6ICN6T7FEM)
- ANEMONE AMERICANA (UNII: 6ICN6T7FEM) (Active Moiety)
- STAR ANISE (UNII: XKC1657P78)
- STAR ANISE (UNII: XKC1657P78) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U) (Active Moiety)
- NAPHTHALENE (UNII: 2166IN72UN)
- NAPHTHALENE (UNII: 2166IN72UN) (Active Moiety)
- SODIUM SULFIDE NONAHYDRATE (UNII: C02T02993U)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- STACHYS OFFICINALIS (UNII: UO9989Y17N)
- STACHYS OFFICINALIS (UNII: UO9989Y17N) (Active Moiety)
- ASPIDOSPERMA QUEBRACHO-BLANCO BARK (UNII: 52B1340190)
- ASPIDOSPERMA QUEBRACHO-BLANCO BARK (UNII: 52B1340190) (Active Moiety)
Which are Bhi Cough 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:
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
Which are the Pharmacologic Classes for Bhi Cough?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Insect Proteins - [CS]
- Non-Standardized Insect Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [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".