NDC 83027-0071 Vax Sode
Thuja Occidentalis,Calcarea Carbonica,Silicea,Salmonella Typhi Nosode,Serum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 83027-0071?
What are the uses for Vax Sode?
What are Vax Sode Active Ingredients?
- ANGUILLA ROSTRATA BLOOD SERUM 18 [hp_X]/mL
- CLOSTRIDIUM TETANI 30 [hp_X]/mL - The cause of TETANUS in humans and domestic animals. It is a common inhabitant of human and horse intestines as well as soil. Two components make up its potent exotoxin activity, a neurotoxin and a hemolytic toxin.
- MEASLES VIRUS 30 [hp_X]/mL - The type species of MORBILLIVIRUS and the cause of the highly infectious human disease MEASLES, which affects mostly children.
- MUMPS VIRUS 30 [hp_X]/mL - The type species of RUBULAVIRUS that causes an acute infectious disease in humans, affecting mainly children. Transmission occurs by droplet infection.
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 9 [hp_X]/mL
- RUBELLA VIRUS 30 [hp_X]/mL - The type (and only) species of RUBIVIRUS causing acute infection in humans, primarily children and young adults. Humans are the only natural host. A live, attenuated vaccine is available for prophylaxis.
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS 18 [hp_C]/mL
- SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI 18 [hp_X]/mL
- SILICON DIOXIDE 9 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/mL
- VACCINIA VIRUS 30 [hp_X]/mL - The type species of ORTHOPOXVIRUS, related to COWPOX VIRUS, but whose true origin is unknown. It has been used as a live vaccine against SMALLPOX. It is also used as a vector for inserting foreign DNA into animals. Rabbitpox virus is a subspecies of VACCINIA VIRUS.
- YERSINIA ENTEROCOLITICA 30 [hp_X]/mL - A species of the genus YERSINIA, isolated from both man and animal. It is a frequent cause of bacterial gastroenteritis in children.
Which are Vax Sode UNII Codes?
The UNII codes for the active ingredients in this product are:
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O)
- SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O) (Active Moiety)
- ANGUILLA ROSTRATA BLOOD SERUM (UNII: L7B16ESD1U)
- ANGUILLA ROSTRATA BLOOD SERUM (UNII: L7B16ESD1U) (Active Moiety)
- CLOSTRIDIUM TETANI (UNII: 751E8J54VM)
- CLOSTRIDIUM TETANI (UNII: 751E8J54VM) (Active Moiety)
- VACCINIA VIRUS (UNII: JDS6958QAG)
- VACCINIA VIRUS (UNII: JDS6958QAG) (Active Moiety)
- MEASLES VIRUS (UNII: HT3R7C012Q)
- MEASLES VIRUS (UNII: HT3R7C012Q) (Active Moiety)
- MUMPS VIRUS (UNII: YF0S03R447)
- MUMPS VIRUS (UNII: YF0S03R447) (Active Moiety)
- RUBELLA VIRUS (UNII: U751HEX436)
- RUBELLA VIRUS (UNII: U751HEX436) (Active Moiety)
- YERSINIA ENTEROCOLITICA (UNII: AUL7Y5Z806)
- YERSINIA ENTEROCOLITICA (UNII: AUL7Y5Z806) (Active Moiety)
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4)
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4) (Active Moiety)
Which are Vax Sode 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)
* 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".