43857-0534 NDC - UNIVERSALTOX (ALFALFA, AVENA SATIVA, FUCUS VESICULOSUS, HORDEUM VULGARE, NASTURTIUM AQUATICUM, RAPHANUS SATIVUS, TRITICUM AESTIVUM, IODIUM, UBIDECARENONUM, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, MANGANESE GLUCONATE, ORYZA SATIVA, THYROIDINUM (SUIS), CALCAREA CARBONICA, NATRUM MURIATICUM, PULSATILLA (PRATENSIS), RHUS TOX, CORTISONE ACETICUM)

Drug Information

  • Product NDC: 43857-0534
  • Proprietary Name: Universaltox
  • Non Proprietary Name: Alfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubidecarenonum, Glandula Suprarenalis Suis, Hepar Suis, Manganese Gluconate, Oryza Sativa, Thyroidinum (Suis), Calcarea Carbonica, Natrum Muriaticum, Pulsatilla (Pratensis), Rhus Tox, Cortisone Aceticum
  • Active Ingredient(s): 3 [hp_X]/mL ALFALFA; 3 [hp_X]/mL AVENA SATIVA FLOWERING TOP; 8 [hp_X]/mL BROWN RICE; 30 [hp_X]/mL CORTISONE ACETATE; 4 [hp_X]/mL DAIKON; 4 [hp_X]/mL FUCUS VESICULOSUS; 4 [hp_X]/mL HORDEUM VULGARE TOP; 6 [hp_X]/mL IODINE; 8 [hp_X]/mL MANGANESE GLUCONATE; 4 [hp_X]/mL NASTURTIUM OFFICINALE; 12 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 8 [hp_X]/mL PORK LIVER; 12 [hp_X]/mL PULSATILLA PRATENSIS WHOLE; 12 [hp_X]/mL SODIUM CHLORIDE; 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND; 8 [hp_X]/mL THYROID; 12 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF; 4 [hp_X]/mL TRITICUM AESTIVUM WHOLE; 6 [hp_X]/mL UBIDECARENONE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]; Dietary Proteins [CS]; Grain Proteins [EXT]; Increased Histamine Release [PE]; Magnetic Resonance Contrast Activity [MoA]; Non-Standardized Food Allergenic Extract [EPC]; Paramagnetic Contrast Agent [EPC]

Labeler Information

Field Name Field Value
Labeler Name: BioActive Nutritional, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/3/2019

Package Information

No. Package Code Package Description Billing Unit
143857-0534-130 mL in 1 BOTTLE, DROPPER (43857-0534-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43857-0534The 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 NAMEUniversaltoxThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAlfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubidecarenonum, Glandula Suprarenalis Suis, Hepar Suis, Manganese Gluconate, Oryza Sativa, Thyroidinum (Suis), Calcarea Carbonica, Natrum Muriaticum, Pulsatilla (Pratensis), Rhus Tox, Cortisone AceticumThe 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 DATE10/3/2019This 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 NAMEBioActive Nutritional, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALFALFA; AVENA SATIVA FLOWERING TOP; BROWN RICE; CORTISONE ACETATE; DAIKON; FUCUS VESICULOSUS; HORDEUM VULGARE TOP; IODINE; MANGANESE GLUCONATE; NASTURTIUM OFFICINALE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PORK LIVER; PULSATILLA PRATENSIS WHOLE; SODIUM CHLORIDE; SUS SCROFA ADRENAL GLAND; THYROID; TOXICODENDRON PUBESCENS LEAF; TRITICUM AESTIVUM WHOLE; UBIDECARENONEAn 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 STRENGTH3; 3; 8; 30; 4; 4; 4; 6; 8; 4; 12; 8; 12; 12; 8; 8; 12; 4; 6 
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; [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], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Magnetic Resonance Contrast Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Paramagnetic Contrast Agent [EPC] 

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This page was last updated on: 7/4/2025

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