Sto Nosode Liquid
NDC 63083-4008
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Sto Nosode is a UNAPPROVED HOMEOPATHIC-approved product labeled by Professional Complementary Health Formulas. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 63083-4008 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
63083-4008
Proprietary Name:
Sto Nosode 4008
Non-Proprietary Name: [1]
Sto Nosode
Substance Name: [2]
Chlamydia Trachomatis; Gardnerella Vaginalis; Gonorrheal Urethral Secretion Human; Proteus Vulgaris; Pseudomonas Aeruginosa; Treponemic Skin Canker Human; Trichomonas Vaginalis
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Liquid
- A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
63083
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]
08-15-1984
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 63083-4008?
The NDC code 63083-4008 is assigned by the FDA to the product Sto Nosode 4008. This pharmaceutical product is labeled by Professional Complementary Health Formulas and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 63083-4008-2. 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?
For the temporary relief of mild skin rash, itchy skin, changes in urination, chills, joint pain or body aches, nausea, or fatigue.*
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.
- CHLAMYDIA TRACHOMATIS 30 [hp_X]/59mL - Type species of CHLAMYDIA causing a variety of ocular and urogenital diseases.
- GARDNERELLA VAGINALIS 30 [hp_X]/59mL - A species in the genus GARDNERELLA previously classified as Haemophilus vaginalis. This bacterium, also isolated from the female genital tract of healthy women, is implicated in the cause of bacterial vaginosis (VAGINOSIS, BACTERIAL).
- GONORRHEAL URETHRAL SECRETION HUMAN 30 [hp_X]/59mL
- PROTEUS VULGARIS 30 [hp_X]/59mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that occurs in soil, fecal matter, and sewage. It is an opportunistic pathogen and causes cystitis and pyelonephritis.
- PSEUDOMONAS AERUGINOSA 30 [hp_X]/59mL - A species of gram-negative, aerobic, rod-shaped bacteria commonly isolated from clinical specimens (wound, burn, and urinary tract infections). It is also found widely distributed in soil and water. P. aeruginosa is a major agent of nosocomial infection.
- TREPONEMIC SKIN CANKER HUMAN 30 [hp_X]/59mL
- TRICHOMONAS VAGINALIS 30 [hp_X]/59mL - A species of TRICHOMONAS that produces a refractory vaginal discharge in females, as well as bladder and urethral infections in males.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLAMYDIA TRACHOMATIS (UNII: T6NI39QU44)
- CHLAMYDIA TRACHOMATIS (UNII: T6NI39QU44) (Active Moiety)
- GARDNERELLA VAGINALIS (UNII: 238RQ26259)
- GARDNERELLA VAGINALIS (UNII: 238RQ26259) (Active Moiety)
- GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F)
- GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F) (Active Moiety)
- PROTEUS VULGARIS (UNII: 11T9HCO30O)
- PROTEUS VULGARIS (UNII: 11T9HCO30O) (Active Moiety)
- PSEUDOMONAS AERUGINOSA (UNII: Y793W5V55N)
- PSEUDOMONAS AERUGINOSA (UNII: Y793W5V55N) (Active Moiety)
- TREPONEMIC SKIN CANKER HUMAN (UNII: 4ZWP7FWI8W)
- TREPONEMIC SKIN CANKER HUMAN (UNII: 4ZWP7FWI8W) (Active Moiety)
- TRICHOMONAS VAGINALIS (UNII: Q25X3G314L)
- TRICHOMONAS VAGINALIS (UNII: Q25X3G314L) (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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".
