43857-0540 NDC - RADIATION (CAPSICUM ANNUUM, CETRARIA ISLANDICA, FUCUS VESICULOSUS, GLANDULA SUPRARENALIS SUIS, THYROIDINUM (SUIS), CADMIUM IODATUM, HYDRANGEA ARBORESCENS, PHOSPHORICUM ACIDUM, PHOSPHORUS, PULSATILLA (PRATENSIS), STRONTIUM CARBONICUM, URANIUM NITRICUM, X-RAY)

Drug Information

  • Product NDC: 43857-0540
  • Proprietary Name: Radiation
  • Non Proprietary Name: Capsicum Annuum, Cetraria Islandica, Fucus Vesiculosus, Glandula Suprarenalis Suis, Thyroidinum (Suis), Cadmium Iodatum, Hydrangea Arborescens, Phosphoricum Acidum, Phosphorus, Pulsatilla (Pratensis), Strontium Carbonicum, Uranium Nitricum, X-Ray
  • Active Ingredient(s): 30 [hp_X]/mL ALCOHOL, X-RAY EXPOSED (1000 RAD); 12 [hp_X]/mL CADMIUM IODIDE; 3 [hp_X]/mL CAPSICUM; 3 [hp_X]/mL CETRARIA ISLANDICA WHOLE; 3 [hp_X]/mL FUCUS VESICULOSUS; 12 [hp_X]/mL HYDRANGEA ARBORESCENS ROOT; 12 [hp_X]/mL PHOSPHORIC ACID; 12 [hp_X]/mL PHOSPHORUS; 12 [hp_X]/mL PULSATILLA PRATENSIS WHOLE; 12 [hp_X]/mL STRONTIUM CARBONATE; 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND; 8 [hp_X]/mL THYROID; 30 [hp_X]/mL URANYL NITRATE HEXAHYDRATE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Vegetable Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: BioActive Nutritional
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/24/2019
End Marketing Date:3/9/2027

Package Information

No. Package Code Package Description Billing Unit
143857-0540-130 mL in 1 BOTTLE, DROPPER (43857-0540-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43857-0540The 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 NAMERadiationThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECapsicum Annuum, Cetraria Islandica, Fucus Vesiculosus, Glandula Suprarenalis Suis, Thyroidinum (Suis), Cadmium Iodatum, Hydrangea Arborescens, Phosphoricum Acidum, Phosphorus, Pulsatilla (Pratensis), Strontium Carbonicum, Uranium Nitricum, X-RayThe 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 DATE10/24/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE3/9/2027This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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 NAMEBioActive NutritionalName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALCOHOL, X-RAY EXPOSED (1000 RAD); CADMIUM IODIDE; CAPSICUM; CETRARIA ISLANDICA WHOLE; FUCUS VESICULOSUS; HYDRANGEA ARBORESCENS ROOT; PHOSPHORIC ACID; PHOSPHORUS; PULSATILLA PRATENSIS WHOLE; STRONTIUM CARBONATE; SUS SCROFA ADRENAL GLAND; THYROID; URANYL NITRATE HEXAHYDRATEAn 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 STRENGTH30; 12; 3; 3; 3; 12; 12; 12; 12; 12; 8; 8; 30 
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_X]/mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS] 

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This page was last updated on: 12/6/2025

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