NDC 43742-1602 Bio Galium Phase
Caltha Palustris,Clematis Erecta,Galium Aparine,Hedera Helix,Juniperus Communis,Sedum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1602 - Bio Galium Phase
Product Packages
NDC Code 43742-1602-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1602?
What are the uses for Bio Galium Phase?
What are Bio Galium Phase Active Ingredients?
- APIS MELLIFERA 12 [hp_X]/mL
- CALCIUM FLUORIDE 8 [hp_X]/mL - Calcium fluoride. Occurring in nature as the mineral fluorite or fluorspar. It is the primary source of fluorine and its compounds. Pure calcium fluoride is used as a catalyst in dehydration and dehydrogenation and is used to fluoridate drinking water. (From Merck Index, 11th ed)
- CALTHA PALUSTRIS 4 [hp_X]/mL
- CLEMATIS RECTA FLOWERING TOP 4 [hp_X]/mL
- CORTISONE ACETATE 8 [hp_X]/mL - A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726)
- ECHINACEA ANGUSTIFOLIA 5 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- GALIUM APARINE 4 [hp_X]/mL - A genus of herbaceous annual and perennial plants in the family RUBIACEAE.
- GOLD 10 [hp_X]/mL - A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.
- HEDERA HELIX FLOWERING TWIG 4 [hp_X]/mL
- JUNIPER BERRY 4 [hp_X]/mL
- NITRIC ACID 8 [hp_X]/mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
- ONONIS SPINOSA WHOLE 5 [hp_C]/mL
- PHOSPHORUS 8 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
- SEDUM ACRE 4 [hp_X]/mL
- SEMPERVIVUM TECTORUM LEAF 4 [hp_X]/mL
- SILVER 8 [hp_X]/mL - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
- THUJA OCCIDENTALIS LEAFY TWIG 4 [hp_X]/mL
- URTICA URENS 4 [hp_X]/mL
Which are Bio Galium Phase UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALTHA PALUSTRIS (UNII: 6S9317F2UT)
- CALTHA PALUSTRIS (UNII: 6S9317F2UT) (Active Moiety)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (Active Moiety)
- GALIUM APARINE (UNII: Z4B6561488)
- GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)
- HEDERA HELIX FLOWERING TWIG (UNII: 3D10KUA6BM)
- HEDERA HELIX FLOWERING TWIG (UNII: 3D10KUA6BM) (Active Moiety)
- JUNIPER BERRY (UNII: O84B5194RL)
- JUNIPER BERRY (UNII: O84B5194RL) (Active Moiety)
- SEDUM ACRE (UNII: 2496VW6S9J)
- SEDUM ACRE (UNII: 2496VW6S9J) (Active Moiety)
- SEMPERVIVUM TECTORUM LEAF (UNII: 3DGJ7BUA01)
- SEMPERVIVUM TECTORUM LEAF (UNII: 3DGJ7BUA01) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- CORTISONE ACETATE (UNII: 883WKN7W8X)
- CORTISONE (UNII: V27W9254FZ) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ONONIS SPINOSA WHOLE (UNII: RP8496915M)
- ONONIS CAMPESTRIS (UNII: RP8496915M) (Active Moiety)
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4)
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4) (Active Moiety)
Which are Bio Galium Phase 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 Galium Phase?
- Allergens - [CS]
- Allergens - [CS]
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
- Corticosteroid - [EPC] (Established Pharmacologic Class)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
* 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".