43742-1279 NDC - DETOX (SOLIDAGO VIRGAUREA, BAPTISIA TINCTORIA, BERBERIS VULGARIS, EQUISETUM HYEMALE, ARGENTUM NITRICUM, CANTHARIS, CAPSICUM ANNUUM, CUPRUM SULPHURICUM, ORTHOSIPHON STAMINEUS, PAREIRA BRAVA, SARSAPARILLA (SMILAX REGELII), APIS VENENUM PURUM, BAROSMA (BETULINA), MERCURIUS CORROSIVUS, PYELON (SUIS), TEREBINTHINA, URETER (SUIS), URETHRA (SUIS), URINARY BLADDER (SUIS), GLYOXAL TRIMER DIHYDRATE, HEPAR SULPHURIS CALCAREUM, NATRUM PYRUVICUM, QUERCETIN, COLIBACILLINUM CUM NATRUM MURIATICUM, DYSENTERY BACILLUS)

Drug Information

Product NDC: 43742-1279

Proprietary Name: Detox

Non Proprietary Name: Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, Equisetum Hyemale, Argentum Nitricum, Cantharis, Capsicum Annuum, Cuprum Sulphuricum, Orthosiphon Stamineus, Pareira Brava, Sarsaparilla (Smilax Regelii), Apis Venenum Purum, Barosma (Betulina), Mercurius Corrosivus, Pyelon (Suis), Terebinthina, Ureter (Suis), Urethra (Suis), Urinary Bladder (Suis), Glyoxal Trimer Dihydrate, Hepar Sulphuris Calcareum, Natrum Pyruvicum, Quercetin, Colibacillinum Cum Natrum Muriaticum, Dysentery Bacillus

Active Ingredient(s):
  • 8 [hp_X]/mL AGATHOSMA BETULINA LEAF;
  • 6 [hp_X]/mL APIS MELLIFERA VENOM;
  • 4 [hp_X]/mL BAPTISIA TINCTORIA ROOT;
  • 4 [hp_X]/mL BERBERIS VULGARIS ROOT BARK;
  • 10 [hp_X]/mL CALCIUM SULFIDE;
  • 6 [hp_X]/mL CAPSICUM;
  • 6 [hp_X]/mL CHONDRODENDRON TOMENTOSUM ROOT;
  • 6 [hp_X]/mL CUPRIC SULFATE;
  • 4 [hp_X]/mL EQUISETUM HYEMALE;
  • 15 [hp_X]/mL ESCHERICHIA COLI;
  • 8 [hp_X]/mL GLYOXAL TRIMER DIHYDRATE;
  • 6 [hp_X]/mL LYTTA VESICATORIA;
  • 8 [hp_X]/mL MERCURIC CHLORIDE;
  • 6 [hp_X]/mL ORTHOSIPHON ARISTATUS WHOLE;
  • 10 [hp_X]/mL QUERCETIN;
  • 30 [hp_C]/mL SHIGELLA DYSENTERIAE;
  • 6 [hp_X]/mL SILVER NITRATE;
  • 6 [hp_X]/mL SMILAX ORNATA ROOT;
  • 10 [hp_X]/mL SODIUM PYRUVATE;
  • 3 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP;
  • 8 [hp_X]/mL SUS SCROFA RENAL PELVIS;
  • 8 [hp_X]/mL SUS SCROFA URETER;
  • 8 [hp_X]/mL SUS SCROFA URETHRA;
  • 8 [hp_X]/mL SUS SCROFA URINARY BLADDER;
  • 8 [hp_X]/mL TURPENTINE OIL


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

Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/25/2018
End Marketing Date:5/8/2024

Package Information

No. Package Code Package Description Billing Unit
143742-1279-130 mL in 1 BOTTLE, DROPPER (43742-1279-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1279The 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 NAMEDetoxThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXIIA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAMESolidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, Equisetum Hyemale, Argentum Nitricum, Cantharis, Capsicum Annuum, Cuprum Sulphuricum, Orthosiphon Stamineus, Pareira Brava, Sarsaparilla (Smilax Regelii), Apis Venenum Purum, Barosma (Betulina), Mercurius Corrosivus, Pyelon (Suis), Terebinthina, Ureter (Suis), Urethra (Suis), Urinary Bladder (Suis), Glyoxal Trimer Dihydrate, Hepar Sulphuris Calcareum, Natrum Pyruvicum, Quercetin, Colibacillinum Cum Natrum Muriaticum, Dysentery BacillusThe 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 DATE9/25/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE5/8/2024This 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 NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAGATHOSMA BETULINA LEAF; APIS MELLIFERA VENOM; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; CALCIUM SULFIDE; CAPSICUM; CHONDRODENDRON TOMENTOSUM ROOT; CUPRIC SULFATE; EQUISETUM HYEMALE; ESCHERICHIA COLI; GLYOXAL TRIMER DIHYDRATE; LYTTA VESICATORIA; MERCURIC CHLORIDE; ORTHOSIPHON ARISTATUS WHOLE; QUERCETIN; SHIGELLA DYSENTERIAE; SILVER NITRATE; SMILAX ORNATA ROOT; SODIUM PYRUVATE; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA RENAL PELVIS; SUS SCROFA URETER; SUS SCROFA URETHRA; SUS SCROFA URINARY BLADDER; TURPENTINE OILAn 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; 6; 4; 4; 10; 6; 6; 6; 4; 15; 8; 6; 8; 6; 10; 30; 6; 6; 10; 3; 8; 8; 8; 8; 8 
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_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 
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: 2/1/2023