Bio Lymph Phase Liquid
NDC 43742-1667
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Bio Lymph Phase (teucrium scorodonia, veronica officinalis, equisetum hyemale, fumaria officinalis, geranium robertianum, nasturtium aquaticum, natrum sulphuricum, pinus sylvestris, gentiana lutea, juglans regia, aranea diadema, sarsaparilla (smilax regelii), ascorbicum acidum, quercetin, scrophularia nodosa, myosotis arvensis, calcarea phosphorica, ferrum iodatum, thyroidinum (suis), gaertner bacillus (bach)) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a ascorbic acid [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-1667 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
43742-1667
Proprietary Name:
Bio Lymph Phase
Non-Proprietary Name: [1]
Teucrium Scorodonia, Veronica Officinalis, Equisetum Hyemale, Fumaria Officinalis, Geranium Robertianum, Nasturtium Aquaticum, Natrum Sulphuricum, Pinus Sylvestris, Gentiana Lutea, Juglans Regia, Aranea Diadema, Sarsaparilla (smilax Regelii), Ascorbicum Acidum, Quercetin, Scrophularia Nodosa, Myosotis Arvensis, Calcarea Phosphorica, Ferrum Iodatum, Thyroidinum (suis), Gaertner Bacillus (bach)
Substance Name: [2]
Araneus Diadematus; Ascorbic Acid; Equisetum Hyemale Whole; Ferrous Iodide; Fumaria Officinalis Flowering Top; Gentiana Lutea Root; Geranium Robertianum Whole; Juglans Regia Leaf; Myosotis Arvensis Whole; Nasturtium Officinale; Pinus Sylvestris Leafy Twig; Quercetin; Salmonella Enterica Enterica Serovar Enteritidis; Scrophularia Nodosa Whole; Smilax Ornata Root; Sodium Sulfate; Teucrium Scorodonia Flowering Top; Thyroid; Tribasic Calcium Phosphate; Veronica Officinalis Flowering Top
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:
43742
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]
08-07-2020
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 43742-1667?
The NDC code 43742-1667 is assigned by the FDA to the product Bio Lymph Phase. It is commonly known by its generic name, teucrium scorodonia, veronica officinalis, equisetum hyemale, fumaria officinalis, geranium robertianum, nasturtium aquaticum, natrum sulphuricum, pinus sylvestris, gentiana lutea, juglans regia, aranea diadema, sarsaparilla (smilax regelii), ascorbicum acidum, quercetin, scrophularia nodosa, myosotis arvensis, calcarea phosphorica, ferrum iodatum, thyroidinum (suis), gaertner bacillus (bach). This pharmaceutical product is labeled by Deseret Biologicals, 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: 43742-1667-1. 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 the temporary relief of swelling due to minor injury.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
For the temporary relief of swelling due to minor injury.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
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.
- ARANEUS DIADEMATUS 6 [hp_X]/mL
- ASCORBIC ACID 6 [hp_X]/mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
- EQUISETUM HYEMALE WHOLE 4 [hp_X]/mL
- FERROUS IODIDE 12 [hp_X]/mL
- FUMARIA OFFICINALIS FLOWERING TOP 4 [hp_X]/mL
- GENTIANA LUTEA ROOT 5 [hp_X]/mL
- GERANIUM ROBERTIANUM WHOLE 4 [hp_X]/mL
- JUGLANS REGIA LEAF 5 [hp_X]/mL
- MYOSOTIS ARVENSIS WHOLE 9 [hp_X]/mL
- NASTURTIUM OFFICINALE 4 [hp_X]/mL - A plant genus of the family BRASSICACEAE. Nasturtium is also used as a common name for TROPAEOLUM. The common name of watercress is also used for RORIPPA & TROPAEOLUM. This is the most popular of the edible cresses, is a hardy creeping perennial plant, native to Europe but extensively naturalized elsewhere in moist places.
- PINUS SYLVESTRIS LEAFY TWIG 4 [hp_X]/mL
- QUERCETIN 6 [hp_X]/mL - A flavonol widely distributed in plants. It is an antioxidant, like many other phenolic heterocyclic compounds. Glycosylated forms include RUTIN and quercetrin.
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
- SCROPHULARIA NODOSA WHOLE 8 [hp_X]/mL
- SMILAX ORNATA ROOT 6 [hp_X]/mL
- SODIUM SULFATE 4 [hp_X]/mL
- TEUCRIUM SCORODONIA FLOWERING TOP 3 [hp_X]/mL
- THYROID 12 [hp_X]/mL - A highly vascularized endocrine gland consisting of two lobes joined by a thin band of tissue with one lobe on each side of the TRACHEA. It secretes THYROID HORMONES from the follicular cells and CALCITONIN from the parafollicular cells thereby regulating METABOLISM and CALCIUM level in blood, respectively.
- TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
- VERONICA OFFICINALIS FLOWERING TOP 3 [hp_X]/mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G)
- TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G) (Active Moiety)
- VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J)
- VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J) (Active Moiety)
- EQUISETUM HYEMALE WHOLE (UNII: 59677RXH25)
- EQUISETUM HYEMALE (UNII: 59677RXH25) (Active Moiety)
- FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL)
- FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (Active Moiety)
- GERANIUM ROBERTIANUM WHOLE (UNII: R5I1HK0UBL)
- GERANIUM ROBERTIANUM (UNII: R5I1HK0UBL) (Active Moiety)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73)
- PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73) (Active Moiety)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
- JUGLANS REGIA LEAF (UNII: 85HKB87105)
- JUGLANS REGIA LEAF (UNII: 85HKB87105) (Active Moiety)
- ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5)
- ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5) (Active Moiety)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG)
- SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- QUERCETIN (UNII: 9IKM0I5T1E)
- QUERCETIN (UNII: 9IKM0I5T1E) (Active Moiety)
- SCROPHULARIA NODOSA WHOLE (UNII: 7H443NUB2T)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
- MYOSOTIS ARVENSIS WHOLE (UNII: C73BK97H5J)
- MYOSOTIS ARVENSIS (UNII: C73BK97H5J) (Active Moiety)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- FERROUS IODIDE (UNII: F5452U54PN)
- FERROUS IODIDE (UNII: F5452U54PN) (Active Moiety)
- THYROID, PORCINE (UNII: 6RV024OAUQ)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4)
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4) (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.
- Ascorbic Acid - [CS]
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Vitamin C - [EPC] (Established Pharmacologic Class)
* 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".
