NDC 83027-0117 Bio Detox Formula
Eucalyptus Globulus,Aloe,Hydrastis Canadensis,Allium Sativum,Alternaria Tenuis - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 83027-0117?
What are the uses for Bio Detox Formula?
What are Bio Detox Formula Active Ingredients?
- ALOE 4 [hp_X]/mL - A plant genus of the family ASPHODELACEAE which is used medicinally. It contains anthraquinone glycosides such as aloin-emodin or aloe-emodin (EMODIN).
- ALTERNARIA ALTERNATA 16 [hp_X]/mL
- ASPERGILLUS NIGER VAR. NIGER 16 [hp_X]/mL
- CANIS LUPUS FAMILIARIS MILK 30 [hp_X]/mL
- CLOSTRIDIUM TETANI 16 [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.
- COW MILK 30 [hp_X]/mL
- DELPHINIUM STAPHISAGRIA SEED 16 [hp_X]/mL
- EUCALYPTOL 20 [hp_X]/mL - A monoterpene and cyclohexanol derivative that is the major component of EUCALYPTUS OIL. It is used in mouthwash, insect repellent, and as a cough suppressant, and also is widely used as a flavoring agent and solvent. It has antimicrobial properties.
- EUCALYPTUS GLOBULUS LEAF 3 [hp_X]/mL
- GARLIC 6 [hp_X]/mL - A species of Allium used as a spice (SPICES) and traditional remedy. It contains alliin lyase and alliin, which is converted by alliin lyase to allicin, the pungent ingredient responsible for the aroma of fresh cut garlic.
- GOLDENSEAL 6 [hp_X]/mL
- RANCID BEEF 20 [hp_X]/mL
- STAPHYLOCOCCUS AUREUS 16 [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 PNEUMONIAE 16 [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 16 [hp_X]/mL
- YERSINIA PESTIS 18 [hp_C]/mL - The etiologic agent of PLAGUE in man, rats, ground squirrels, and other rodents.
Which are Bio Detox Formula UNII Codes?
The UNII codes for the active ingredients in this product are:
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (Active Moiety)
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- GARLIC (UNII: V1V998DC17)
- GARLIC (UNII: V1V998DC17) (Active Moiety)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (Active Moiety)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
- CLOSTRIDIUM TETANI (UNII: 751E8J54VM)
- CLOSTRIDIUM TETANI (UNII: 751E8J54VM) (Active Moiety)
- STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2)
- STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2) (Active Moiety)
- STAPHYLOCOCCUS AUREUS (UNII: O478WX4004)
- STAPHYLOCOCCUS AUREUS (UNII: O478WX4004) (Active Moiety)
- STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR)
- STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
- EUCALYPTOL (UNII: RV6J6604TK)
- EUCALYPTOL (UNII: RV6J6604TK) (Active Moiety)
- RANCID BEEF (UNII: 29SUH5R3HU)
- RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
- CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT)
- CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT) (Active Moiety)
- COW MILK (UNII: 917J3173FT)
- COW MILK (UNII: 917J3173FT) (Active Moiety)
- YERSINIA PESTIS (UNII: S6JJH3XV1D)
- YERSINIA PESTIS (UNII: S6JJH3XV1D) (Active Moiety)
Which are Bio Detox Formula 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)
Which are the Pharmacologic Classes for Bio Detox Formula?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Fungal Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Milk Proteins - [CS]
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
* 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".