57520-0757 NDC - LYMPH (CEANOTHUS AMERICANUS, EUPHRASIA OFFICINALIS, GERMANIUM ROBERTIANUM,)

Drug Information

Product NDC: 57520-0757

Proprietary Name: Lymph

Non Proprietary Name: Ceanothus Americanus, Euphrasia Officinalis, Germanium Robertianum,

Active Ingredient(s):
  • 1 [hp_X]/mL CEANOTHUS AMERICANUS LEAF;
  • 1 [hp_X]/mL EUPHRASIA STRICTA;
  • 1 [hp_X]/mL GERANIUM ROBERTIANUM;
  • 1 [hp_X]/mL JUGLANS REGIA FLOWERING TOP;
  • 1 [hp_X]/mL MYOSOTIS ARVENSIS;
  • 1 [hp_X]/mL SMILAX REGELII ROOT;
  • 1 [hp_X]/mL SCROPHULARIA NODOSA;
  • 1 [hp_X]/mL TEUCRIUM SCORODONIA FLOWERING TOP;
  • 1 [hp_X]/mL ALTHAEA OFFICINALIS ROOT;
  • 1 [hp_X]/mL PEUMUS BOLDUS LEAF;
  • 1 [hp_X]/mL CALENDULA OFFICINALIS FLOWERING TOP;
  • 1 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG;
  • 1 [hp_X]/mL FUMARIA OFFICINALIS FLOWERING TOP;
  • 1 [hp_X]/mL PINUS SYLVESTRIS LEAFY TWIG;
  • 1 [hp_X]/mL GENTIANA LUTEA ROOT;
  • 1 [hp_X]/mL POTASSIUM IODIDE;
  • 1 [hp_X]/mL ECHINACEA, UNSPECIFIED;
  • 3 [hp_X]/mL RORIPPA NASTURTIUM-AQUATICUM;
  • 3 [hp_X]/mL VISCUM ALBUM FRUITING TOP;
  • 3 [hp_X]/mL PHYTOLACCA AMERICANA ROOT;
  • 3 [hp_X]/mL CAPSICUM;
  • 4 [hp_X]/mL VERONICA OFFICINALIS FLOWERING TOP;
  • 4 [hp_X]/mL APIS MELLIFERA;
  • 4 [hp_X]/mL EQUISETUM HYEMALE;
  • 4 [hp_X]/mL SODIUM SULFATE;
  • 8 [hp_X]/mL BARIUM CARBONATE;
  • 8 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE;
  • 8 [hp_X]/mL CALCIUM SULFIDE;
  • 8 [hp_X]/mL FERROUS IODIDE;
  • 8 [hp_X]/mL MERCURIC CYANIDE;
  • 12 [hp_X]/mL ARANEUS DIADEMATUS;
  • 12 [hp_X]/mL SUS SCROFA PARATHYROID GLAND;
  • 12 [hp_X]/mL SUS SCROFA THYMUS;
  • 12 [hp_X]/mL THYROID, PORCINE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/12/2011

Package Information

No. Package Code Package Description Billing Unit
157520-0757-130 mL in 1 BOTTLE, DROPPER (57520-0757-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57520-0757The 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 NAMELymphThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXRxA 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 NAMECeanothus Americanus, Euphrasia Officinalis, Germanium Robertianum,The 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 DATE9/12/2011This 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 NAMEApotheca CompanyName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECEANOTHUS AMERICANUS LEAF; EUPHRASIA STRICTA; GERANIUM ROBERTIANUM; JUGLANS REGIA FLOWERING TOP; MYOSOTIS ARVENSIS; SMILAX REGELII ROOT; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; ALTHAEA OFFICINALIS ROOT; PEUMUS BOLDUS LEAF; CALENDULA OFFICINALIS FLOWERING TOP; THUJA OCCIDENTALIS LEAFY TWIG; FUMARIA OFFICINALIS FLOWERING TOP; PINUS SYLVESTRIS LEAFY TWIG; GENTIANA LUTEA ROOT; POTASSIUM IODIDE; ECHINACEA, UNSPECIFIED; RORIPPA NASTURTIUM-AQUATICUM; VISCUM ALBUM FRUITING TOP; PHYTOLACCA AMERICANA ROOT; CAPSICUM; VERONICA OFFICINALIS FLOWERING TOP; APIS MELLIFERA; EQUISETUM HYEMALE; SODIUM SULFATE; BARIUM CARBONATE; TRIBASIC CALCIUM PHOSPHATE; CALCIUM SULFIDE; FERROUS IODIDE; MERCURIC CYANIDE; ARANEUS DIADEMATUS; SUS SCROFA PARATHYROID GLAND; SUS SCROFA THYMUS; THYROID, PORCINEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH1; 1; 1; 1; 1; 1; 1; 1; 1; 1; 1; 1; 1; 1; 1; 1; 1; 3; 3; 3; 3; 4; 4; 4; 4; 8; 8; 8; 8; 8; 12; 12; 12; 12 
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; [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 

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