Vax Sode Spray
NDC 83027-0071
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Vax Sode (thuja occidentalis, calcarea carbonica, silicea, salmonella typhi nosode, serum anguillae, bacillus tetani(clostridium tetani), malandrinum, morbillinum, parotidinum, rubella nosode, yersinia enterocolitica, salmonella enteriditis) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Nutritional Specialties, Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a spray for oral administration. This product entry covers the primary NDC 83027-0071 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
83027-0071
Proprietary Name:
Vax Sode
Non-Proprietary Name: [1]
Thuja Occidentalis, Calcarea Carbonica, Silicea, Salmonella Typhi Nosode, Serum Anguillae, Bacillus Tetani(clostridium Tetani), Malandrinum, Morbillinum, Parotidinum, Rubella Nosode, Yersinia Enterocolitica, Salmonella Enteriditis
Substance Name: [2]
Anguilla Rostrata Blood Serum; Clostridium Tetani; Measles Virus; Mumps Virus; Oyster Shell Calcium Carbonate, Crude; Rubella Virus; Salmonella Enterica Enterica Serovar Enteritidis; Salmonella Enterica Enterica Serovar Typhi; Silicon Dioxide; Thuja Occidentalis Leafy Twig; Vaccinia Virus; Yersinia Enterocolitica
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Spray
- A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
83027
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
09-11-2023
End Marketing Date: [10]
09-21-2028
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 83027-0071?
The NDC code 83027-0071 is assigned by the FDA to the product Vax Sode. It is commonly known by its generic name, thuja occidentalis, calcarea carbonica, silicea, salmonella typhi nosode, serum anguillae, bacillus tetani(clostridium tetani), malandrinum, morbillinum, parotidinum, rubella nosode, yersinia enterocolitica, salmonella enteriditis. This pharmaceutical product is labeled by Nutritional Specialties, Inc. and is currently categorized as listed product. The medication is a spray administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 83027-0071-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage.For high sensitive individuals: best tolerated administration is through imbrication (RUBBING IN) on skin at pulse points or abdomen.Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.
What are Active Ingredients of this product?
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.
- 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 the associated 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 the Inactive Ingredients associated 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)
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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
