Septaforce Liquid
NDC 43857-0620
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Septaforce (baptisia tinctoria, echinacea (angustifolia), arsenicum album, chininum sulphuricum, crotalus horridus, lachesis mutus, secale cornutum, tarentula cubensis, latrodectus mactans, anthracinum, loxosceles reclusa) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Bioactive Nutritional, Inc.. This medication is typically used as a antimalarial [epc]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43857-0620 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
43857-0620
Proprietary Name:
Septaforce
Non-Proprietary Name: [1]
Baptisia Tinctoria, Echinacea (angustifolia), Arsenicum Album, Chininum Sulphuricum, Crotalus Horridus, Lachesis Mutus, Secale Cornutum, Tarentula Cubensis, Latrodectus Mactans, Anthracinum, Loxosceles Reclusa
Substance Name: [2]
Arsenic Trioxide; Bacillus Anthracis Immunoserum Rabbit; Baptisia Tinctoria Root; Citharacanthus Spinicrus; Claviceps Purpurea Sclerotium; Crotalus Horridus Horridus Venom; Echinacea Angustifolia Whole; Lachesis Muta Venom; Latrodectus Mactans; Loxosceles Reclusa; Quinine Sulfate
NDC Directory Status:
Human Prescription 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:
43857
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]
11-19-2021
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 43857-0620?
The NDC code 43857-0620 is assigned by the FDA to the product Septaforce. It is commonly known by its generic name, baptisia tinctoria, echinacea (angustifolia), arsenicum album, chininum sulphuricum, crotalus horridus, lachesis mutus, secale cornutum, tarentula cubensis, latrodectus mactans, anthracinum, loxosceles reclusa. This pharmaceutical product is labeled by Bioactive Nutritional, Inc. 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: 43857-0620-1. 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?
For temporary relief of constricted feeling of the chest, palpitations with anxiety, purplish hue, burning, stinging pains, inflammation of connective tissues.
For temporary relief of constricted feeling of the chest, palpitations with anxiety, purplish hue, burning, stinging pains, inflammation of connective tissues.
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.
- ARSENIC TRIOXIDE 12 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT 33 [hp_X]/mL
- BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
- CITHARACANTHUS SPINICRUS 12 [hp_X]/mL
- CLAVICEPS PURPUREA SCLEROTIUM 12 [hp_X]/mL
- CROTALUS HORRIDUS HORRIDUS VENOM 12 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- LATRODECTUS MACTANS 12 [hp_X]/mL
- LOXOSCELES RECLUSA 15 [hp_C]/mL - A spider of the genus Loxosceles, found in the midwestern and other parts of the United States, which carries a hemolytic venom that produces local necrosis or ulceration.
- QUININE SULFATE 12 [hp_X]/mL - An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- QUININE SULFATE (UNII: KF7Z0E0Q2B)
- QUININE (UNII: A7V27PHC7A) (Active Moiety)
- CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956)
- CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
- CITHARACANTHUS SPINICRUS (UNII: 3Y5X6RT823)
- CITHARACANTHUS SPINICRUS (UNII: 3Y5X6RT823) (Active Moiety)
- LATRODECTUS MACTANS (UNII: XJJ7QA858R)
- LATRODECTUS MACTANS (UNII: XJJ7QA858R) (Active Moiety)
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N)
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (Active Moiety)
- LOXOSCELES RECLUSA (UNII: 039G4OZ3G2)
- LOXOSCELES RECLUSA (UNII: 039G4OZ3G2) (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)
Which are the Pharmacologic Classes of this product?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
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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 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".
