NDC 62106-6870 Muco Coccinum
Klebsiella Pneumoniae Tablet Sublingual - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62106 - Seroyal Usa
- 62106-6870 - Muco Coccinum
Product Characteristics
Product Packages
NDC Code 62106-6870-0
Package Description: 1 BLISTER PACK in 1 BOX / 10 TABLET in 1 BLISTER PACK
Product Details
What is NDC 62106-6870?
What are the uses for Muco Coccinum?
What are Muco Coccinum Active Ingredients?
- ANAEROCOCCUS TETRADIUS 200 [hp_C]/1
- INFLUENZA A VIRUS 200 [hp_C]/1 - The type species of the genus ALPHAINFLUENZAVIRUS that causes influenza and other diseases in humans and animals. Antigenic variation occurs frequently between strains, allowing classification into subtypes and variants. Transmission is usually by aerosol (human and most non-aquatic hosts) or waterborne (ducks). Infected birds shed the virus in their saliva, nasal secretions, and feces.
- INFLUENZA B VIRUS 200 [hp_C]/1 - Species of the genus BETAINFLUENZAVIRUS that cause HUMAN INFLUENZA and other diseases primarily in humans. Antigenic variation is less extensive than in type A viruses (INFLUENZA A VIRUS) and consequently there is no basis for distinct subtypes or variants. Epidemics are less likely than with INFLUENZA A VIRUS and there have been no pandemics. Previously only found in humans, Influenza B virus has been isolated from seals which may constitute the animal reservoir from which humans are exposed.
- KLEBSIELLA PNEUMONIAE 200 [hp_C]/1 - Gram-negative, non-motile, capsulated, gas-producing rods found widely in nature and associated with urinary and respiratory infections in humans.
- MORAXELLA CATARRHALIS SUBSP. CATARRHALIS 200 [hp_C]/1
Which are Muco Coccinum UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANAEROCOCCUS TETRADIUS (UNII: 7Q9DHH4FGG)
- ANAEROCOCCUS TETRADIUS (UNII: 7Q9DHH4FGG) (Active Moiety)
- INFLUENZA A VIRUS (UNII: R9HH0NDE2E)
- INFLUENZA A VIRUS (UNII: R9HH0NDE2E) (Active Moiety)
- INFLUENZA B VIRUS (UNII: 1314JZ2X6W)
- INFLUENZA B VIRUS (UNII: 1314JZ2X6W) (Active Moiety)
- KLEBSIELLA PNEUMONIAE (UNII: 09PA36CT5R)
- KLEBSIELLA PNEUMONIAE (UNII: 09PA36CT5R) (Active Moiety)
- MORAXELLA CATARRHALIS SUBSP. CATARRHALIS (UNII: 1X259JGO78)
- MORAXELLA CATARRHALIS SUBSP. CATARRHALIS (UNII: 1X259JGO78) (Active Moiety)
Which are Muco Coccinum 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- XYLITOL (UNII: VCQ006KQ1E)
* 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.
[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".