43742-2207 NDC - CHRONAGESIC (ALPHA-LIPOICUM ACIDUM, APIOLUM, ARNICA MONTANA, CARTILAGO SUIS, CINNAMOMUM, DULCAMARA, FUNICULUS UMBILICALIS SUIS, NADIDUM, NATRUM OXALACETICUM, PANTOTHENIC ACID, PLACENTA TOTALIS SUIS, PIPER NIGRUM, RHUS TOX, SANGUINARIA CANADENSIS, SULPHUR, SILICEA, SYMPHYTUM OFFICINALE, THUJA OCCIDENTALIS)

Drug Information

  • Product NDC: 43742-2207
  • Proprietary Name: Chronagesic
  • Non Proprietary Name: Alpha-Lipoicum Acidum, Apiolum, Arnica Montana, Cartilago Suis, Cinnamomum, Dulcamara, Funiculus Umbilicalis Suis, Nadidum, Natrum Oxalaceticum, Pantothenic Acid, Placenta Totalis Suis, Piper Nigrum, Rhus Tox, Sanguinaria Canadensis, Sulphur, Silicea, Symphytum Officinale, Thuja Occidentalis
  • Active Ingredient(s): 8 [hp_X]/mL ALPHA LIPOIC ACID; 16 [hp_C]/mL APIOLE (PARSLEY); 3 [hp_X]/mL ARNICA MONTANA WHOLE; 6 [hp_X]/mL CINNAMON; 8 [hp_X]/mL COMFREY ROOT; 6 [hp_X]/mL GREEN PEPPERCORN; 6 [hp_X]/mL NADIDE; 6 [hp_X]/mL PANTOTHENIC ACID; 6 [hp_X]/mL SANGUINARIA CANADENSIS ROOT; 8 [hp_X]/mL SILICON DIOXIDE; 6 [hp_X]/mL SODIUM DIETHYL OXALACETATE; 6 [hp_X]/mL SOLANUM DULCAMARA TOP; 6 [hp_X]/mL SULFUR; 8 [hp_X]/mL SUS SCROFA CARTILAGE; 6 [hp_X]/mL SUS SCROFA PLACENTA; 6 [hp_X]/mL SUS SCROFA UMBILICAL CORD; 12 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG; 8 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Food Additives [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:11/8/2024

Package Information

No. Package Code Package Description Billing Unit
143742-2207-130 mL in 1 BOTTLE, DROPPER (43742-2207-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2207The 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 NAMEChronagesicThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAlpha-Lipoicum Acidum, Apiolum, Arnica Montana, Cartilago Suis, Cinnamomum, Dulcamara, Funiculus Umbilicalis Suis, Nadidum, Natrum Oxalaceticum, Pantothenic Acid, Placenta Totalis Suis, Piper Nigrum, Rhus Tox, Sanguinaria Canadensis, Sulphur, Silicea, Symphytum Officinale, Thuja OccidentalisThe 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 DATE11/8/2024This 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 NAMEALPHA LIPOIC ACID; APIOLE (PARSLEY); ARNICA MONTANA WHOLE; CINNAMON; COMFREY ROOT; GREEN PEPPERCORN; NADIDE; PANTOTHENIC ACID; SANGUINARIA CANADENSIS ROOT; SILICON DIOXIDE; SODIUM DIETHYL OXALACETATE; SOLANUM DULCAMARA TOP; SULFUR; SUS SCROFA CARTILAGE; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAFAn 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 STRENGTH8; 16; 3; 6; 8; 6; 6; 6; 6; 8; 6; 6; 6; 8; 6; 6; 12; 8 
ACTIVE INGRED UNIT[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; [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 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC] 

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This page was last updated on: 2/5/2026

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