60986-1004 NDC - LYMPHONEST (ECHINACEA AUGUSTIFOLIA, SCROPHULARIA NODOSA, ABROTANUM, PETROLEUM, ALOE SOCOTRINA, MERCURIUS SOLUBILIS, CROTALUS HORIIDUS, THUJA OCCIDENTALIS, LACHESIS MUTUS, ARISTOLOCHIA CLEMATITIS)

Drug Information

Product NDC: 60986-1004

Proprietary Name: Lymphonest

Non Proprietary Name: Echinacea augustifolia, Scrophularia nodosa, Abrotanum, Petroleum, Aloe socotrina, Mercurius solubilis, Crotalus horiidus, Thuja occidentalis, Lachesis mutus, Aristolochia clematitis

Active Ingredient(s):
  • 1 [hp_X]/100mL ECHINACEA ANGUSTIFOLIA;
  • 1 [hp_X]/100mL SCROPHULARIA NODOSA;
  • 3 [hp_X]/100mL ARTEMISIA ABROTANUM FLOWERING TOP;
  • 3 [hp_X]/100mL KEROSENE;
  • 1 [hp_X]/100mL ALOE;
  • 12 [hp_X]/100mL MERCURIUS SOLUBILIS;
  • 10 [hp_X]/100mL CROTALUS HORRIDUS HORRIDUS VENOM;
  • 10 [hp_X]/100mL THUJA OCCIDENTALIS LEAFY TWIG;
  • 8 [hp_X]/100mL LACHESIS MUTA VENOM;
  • 6 [hp_X]/100mL ARISTOLOCHIA CLEMATITIS ROOT


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: Marco Pharma International LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/1/1992

Package Information

No. Package Code Package Description Billing Unit
160986-1004-350 mL in 1 BOTTLE, GLASS (60986-1004-3)
260986-1004-4100 mL in 1 PACKAGE (60986-1004-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC60986-1004The 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 NAMELymphonestThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEEchinacea augustifolia, Scrophularia nodosa, Abrotanum, Petroleum, Aloe socotrina, Mercurius solubilis, Crotalus horiidus, Thuja occidentalis, Lachesis mutus, Aristolochia clematitisThe 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 DATE3/1/1992This 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 NAMEMarco Pharma International LLC.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEECHINACEA ANGUSTIFOLIA; SCROPHULARIA NODOSA; ARTEMISIA ABROTANUM FLOWERING TOP; KEROSENE; ALOE; MERCURIUS SOLUBILIS; CROTALUS HORRIDUS HORRIDUS VENOM; THUJA OCCIDENTALIS LEAFY TWIG; LACHESIS MUTA VENOM; ARISTOLOCHIA CLEMATITIS ROOTThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH1; 1; 3; 3; 1; 12; 10; 10; 8; 6 
ACTIVE INGRED UNIT[hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL 

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