58048-0001 NDC - LYME AND CO-INFECTION NOSODE (ANGELICA ARCHANGELICA, HYDRASTIS CANADENSIS, KALI MURIATICUM, YUCCA FILAMENTOSA, CARTILAGO SUIS, PHYTOLACCA DECANDRA, RHUS TOXICODENDRON)

Drug Information

Product NDC: 58048-0001

Proprietary Name: Lyme and Co-Infection Nosode

Non Proprietary Name: Angelica Archangelica, Hydrastis Canadensis, Kali Muriaticum, Yucca Filamentosa, Cartilago Suis, Phytolacca Decandra, Rhus Toxicodendron

Active Ingredient(s):
  • 2 [hp_X]/mL ANGELICA ARCHANGELICA ROOT;
  • 3 [hp_X]/mL GOLDENSEAL;
  • 3 [hp_X]/mL POTASSIUM CHLORIDE;
  • 3 [hp_X]/mL YUCCA FILAMENTOSA;
  • 3 [hp_X]/mL SUS SCROFA CARTILAGE;
  • 3 [hp_X]/mL PHYTOLACCA AMERICANA ROOT;
  • 6 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF;
  • 6 [hp_X]/mL CAUSTICUM;
  • 8 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE;
  • 8 [hp_X]/mL MANGANESE;
  • 8 [hp_X]/mL OXALIC ACID;
  • 8 [hp_X]/mL ARNICA MONTANA;
  • 12 [hp_X]/mL CHLAMYDIA TRACHOMATIS;
  • 12 [hp_X]/mL BABESIA MICROTI;
  • 12 [hp_X]/mL BORRELIA BURGDORFERI;
  • 12 [hp_X]/mL LATRODECTUS MACTANS;
  • 6 [hp_C]/mL ANHYDROUS CITRIC ACID;
  • 6 [hp_C]/mL HUMAN HERPESVIRUS 5;
  • 8 [hp_C]/mL RICKETTSIA RICKETTSII;
  • 12 [hp_C]/mL JAPANESE ENCEPHALITIS VIRUS;
  • 30 [hp_C]/mL LEDUM PALUSTRE TWIG


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: BioPure Healing Products, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/4/2013
End Marketing Date:9/28/2021

Package Information

No. Package Code Package Description Billing Unit
158048-0001-160 mL in 1 BOTTLE, DROPPER (58048-0001-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC58048-0001The 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 NAMELyme and Co-Infection NosodeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAngelica Archangelica, Hydrastis Canadensis, Kali Muriaticum, Yucca Filamentosa, Cartilago Suis, Phytolacca Decandra, Rhus ToxicodendronThe 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 DATE10/4/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE9/28/2021This 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 NAMEBioPure Healing Products, LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEANGELICA ARCHANGELICA ROOT; GOLDENSEAL; POTASSIUM CHLORIDE; YUCCA FILAMENTOSA; SUS SCROFA CARTILAGE; PHYTOLACCA AMERICANA ROOT; TOXICODENDRON PUBESCENS LEAF; CAUSTICUM; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MANGANESE; OXALIC ACID; ARNICA MONTANA; CHLAMYDIA TRACHOMATIS; BABESIA MICROTI; BORRELIA BURGDORFERI; LATRODECTUS MACTANS; ANHYDROUS CITRIC ACID; HUMAN HERPESVIRUS 5; RICKETTSIA RICKETTSII; JAPANESE ENCEPHALITIS VIRUS; LEDUM PALUSTRE TWIGThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH2; 3; 3; 3; 3; 3; 6; 6; 8; 8; 8; 8; 12; 12; 12; 12; 6; 6; 8; 12; 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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL 

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This page was last updated on: 9/13/2019