43742-1667 NDC - 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))

Drug Information

Product NDC: 43742-1667

Proprietary Name: Bio Lymph Phase

Non Proprietary 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)

Active Ingredient(s):
  • 6 [hp_X]/mL ARANEUS DIADEMATUS;
  • 6 [hp_X]/mL ASCORBIC ACID;
  • 4 [hp_X]/mL EQUISETUM HYEMALE WHOLE;
  • 12 [hp_X]/mL FERROUS IODIDE;
  • 4 [hp_X]/mL FUMARIA OFFICINALIS FLOWERING TOP;
  • 5 [hp_X]/mL GENTIANA LUTEA ROOT;
  • 4 [hp_X]/mL GERANIUM ROBERTIANUM WHOLE;
  • 5 [hp_X]/mL JUGLANS REGIA LEAF;
  • 9 [hp_X]/mL MYOSOTIS ARVENSIS WHOLE;
  • 4 [hp_X]/mL NASTURTIUM OFFICINALE;
  • 4 [hp_X]/mL PINUS SYLVESTRIS LEAFY TWIG;
  • 6 [hp_X]/mL QUERCETIN;
  • 30 [hp_C]/mL SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS;
  • 8 [hp_X]/mL SCROPHULARIA NODOSA WHOLE;
  • 6 [hp_X]/mL SMILAX ORNATA ROOT;
  • 4 [hp_X]/mL SODIUM SULFATE;
  • 3 [hp_X]/mL TEUCRIUM SCORODONIA FLOWERING TOP;
  • 12 [hp_X]/mL THYROID, PORCINE;
  • 12 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE;
  • 3 [hp_X]/mL VERONICA OFFICINALIS FLOWERING TOP


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Ascorbic Acid [CS];
  • Blood Coagulation Factor [EPC];
  • Calcium [CS];
  • Cations;
  • Divalent [CS];
  • Increased Coagulation Factor Activity [PE];
  • Vitamin C [EPC]

Labeler Information

Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/7/2020

Package Information

No. Package Code Package Description Billing Unit
143742-1667-130 mL in 1 BOTTLE, DROPPER (43742-1667-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1667The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEBio Lymph PhaseThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMETeucrium 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)The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE8/7/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARANEUS 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, PORCINE; TRIBASIC CALCIUM PHOSPHATE; VERONICA OFFICINALIS FLOWERING TOPAn 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.
ACTIVE NUMERATOR STRENGTH6; 6; 4; 12; 4; 5; 4; 5; 9; 4; 4; 6; 30; 8; 6; 4; 3; 12; 12; 3 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAscorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Vitamin C [EPC] 

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This page was last updated on: 2/1/2023