Bacti Sode Spray
NDC 83027-0152
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Bacti Sode (bacillus tetani, chlamydia trachomatis, colibacillinum cum natrum muriaticum, klebsiella pneumoniae, mycobacterium paratuberculosis, mycoplasma pneumoniae, pneumococcinum, salmonella typhi nosode, staphylococcus aureus, streptococcus viridans, pyrogenium, pertussinum, streptococcus agalactiae, streptococcus dysgalactiae, streptococcus mutans, bacillus cereus) 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 83027-0152 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
83027-0152
Proprietary Name:
Bacti Sode
Non-Proprietary Name: [1]
Bacillus Tetani, Chlamydia Trachomatis, Colibacillinum Cum Natrum Muriaticum, Klebsiella Pneumoniae, Mycobacterium Paratuberculosis, Mycoplasma Pneumoniae, Pneumococcinum, Salmonella Typhi Nosode, Staphylococcus Aureus, Streptococcus Viridans, Pyrogenium, Pertussinum, Streptococcus Agalactiae, Streptococcus Dysgalactiae, Streptococcus Mutans, Bacillus Cereus
Substance Name: [2]
Bacillus Cereus; Chlamydia Trachomatis; Clostridium Tetani; Escherichia Coli; Human Sputum, Bordetella Pertussis Infected; Klebsiella Pneumoniae; Mycobacterium Avium Subsp. Paratuberculosis; Mycoplasma Pneumoniae; Rancid Beef; Salmonella Enterica Enterica Serovar Typhi; Staphylococcus Aureus; Streptococcus Agalactiae; Streptococcus Dysgalactiae; Streptococcus Mutans; Streptococcus Pneumoniae; Streptococcus Viridans Group
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]
04-29-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 83027-0152?
The NDC code 83027-0152 is assigned by the FDA to the product Bacti Sode. It is commonly known by its generic name, bacillus tetani, chlamydia trachomatis, colibacillinum cum natrum muriaticum, klebsiella pneumoniae, mycobacterium paratuberculosis, mycoplasma pneumoniae, pneumococcinum, salmonella typhi nosode, staphylococcus aureus, streptococcus viridans, pyrogenium, pertussinum, streptococcus agalactiae, streptococcus dysgalactiae, streptococcus mutans, bacillus cereus. 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: 83027-0152-1. 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.• 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.
- BACILLUS CEREUS 18 [hp_C]/mL - A species of rod-shaped bacteria that is a common soil saprophyte. Its spores are widespread and multiplication has been observed chiefly in foods. Contamination may lead to food poisoning.
- CHLAMYDIA TRACHOMATIS 20 [hp_X]/mL - Type species of CHLAMYDIA causing a variety of ocular and urogenital diseases.
- CLOSTRIDIUM TETANI 20 [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.
- ESCHERICHIA COLI 20 [hp_X]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 30 [hp_X]/mL
- KLEBSIELLA PNEUMONIAE 20 [hp_X]/mL - Gram-negative, non-motile, capsulated, gas-producing rods found widely in nature and associated with urinary and respiratory infections in humans.
- MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS 20 [hp_X]/mL - A subspecies of gram-positive, aerobic bacteria. It is the etiologic agent of Johne's disease (PARATUBERCULOSIS), a chronic GASTROENTERITIS in RUMINANTS.
- MYCOPLASMA PNEUMONIAE 20 [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.
- RANCID BEEF 20 [hp_X]/mL
- SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI 20 [hp_X]/mL
- STAPHYLOCOCCUS AUREUS 20 [hp_X]/mL - Potentially pathogenic bacteria found in nasal membranes, skin, hair follicles, and perineum of warm-blooded animals. They may cause a wide range of infections and intoxications.
- STREPTOCOCCUS AGALACTIAE 15 [hp_C]/mL - A bacterium which causes mastitis in cattle and occasionally in man.
- STREPTOCOCCUS DYSGALACTIAE 15 [hp_C]/mL
- STREPTOCOCCUS MUTANS 15 [hp_C]/mL - A polysaccharide-producing species of STREPTOCOCCUS isolated from human dental plaque.
- STREPTOCOCCUS PNEUMONIAE 20 [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.
- STREPTOCOCCUS VIRIDANS GROUP 20 [hp_X]/mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOSTRIDIUM TETANI (UNII: 751E8J54VM)
- CLOSTRIDIUM TETANI (UNII: 751E8J54VM) (Active Moiety)
- CHLAMYDIA TRACHOMATIS (UNII: T6NI39QU44)
- CHLAMYDIA TRACHOMATIS (UNII: T6NI39QU44) (Active Moiety)
- ESCHERICHIA COLI (UNII: 514B9K0L10)
- ESCHERICHIA COLI (UNII: 514B9K0L10) (Active Moiety)
- KLEBSIELLA PNEUMONIAE (UNII: 09PA36CT5R)
- KLEBSIELLA PNEUMONIAE (UNII: 09PA36CT5R) (Active Moiety)
- MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS (UNII: XH0F4IP2RX)
- MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS (UNII: XH0F4IP2RX) (Active Moiety)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0) (Active Moiety)
- STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2)
- STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2) (Active Moiety)
- SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O)
- SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O) (Active Moiety)
- STAPHYLOCOCCUS AUREUS (UNII: O478WX4004)
- STAPHYLOCOCCUS AUREUS (UNII: O478WX4004) (Active Moiety)
- STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR)
- STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR) (Active Moiety)
- RANCID BEEF (UNII: 29SUH5R3HU)
- RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN)
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN) (Active Moiety)
- STREPTOCOCCUS AGALACTIAE (UNII: 2B3763S671)
- STREPTOCOCCUS AGALACTIAE (UNII: 2B3763S671) (Active Moiety)
- STREPTOCOCCUS DYSGALACTIAE (UNII: LN0SH02Y5M)
- STREPTOCOCCUS DYSGALACTIAE (UNII: LN0SH02Y5M) (Active Moiety)
- STREPTOCOCCUS MUTANS (UNII: 5C7J33MJJ1)
- STREPTOCOCCUS MUTANS (UNII: 5C7J33MJJ1) (Active Moiety)
- BACILLUS CEREUS (UNII: 7YC151N82L)
- BACILLUS CEREUS (UNII: 7YC151N82L) (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)
* Please review the full disclaimer at the bottom of this page.
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 Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
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".
