55714-4545 NDC - LYMPHATIC DRAINER (ASTERIAS RUBENS, AUR. MET.,BELLADONNA, BENZOICUM ACIDUM, BERBER. VULG., BRYONIA, CALC. CARB., CANTHARIS, CEANOTHUS, CHELIDONIUM MAJUS CHIONANTHUS VIRGINICA, CINCHONA, DIOSCOREA ,IRIS VERSICOLOR, NAT. CARB., NUX VOM., PTELEA, CARDUUS MAR., ECHINACEA, SOLIDAGO, TARAXACUM)

Drug Information

Product NDC: 55714-4545

Proprietary Name: Lymphatic Drainer

Non Proprietary Name: Asterias rubens, Aur. met.,Belladonna, Benzoicum acidum, Berber. vulg., Bryonia, Calc. carb., Cantharis, Ceanothus, Chelidonium majus Chionanthus virginica, Cinchona, Dioscorea ,Iris versicolor, Nat. carb., Nux vom., Ptelea, Carduus mar., Echinacea, Solidago, Taraxacum

Active Ingredient(s):
  • 15 [hp_X]/g ASTERIAS RUBENS;
  • 15 [hp_X]/g GOLD;
  • 15 [hp_X]/g ATROPA BELLADONNA;
  • 15 [hp_X]/g BENZOIC ACID;
  • 15 [hp_X]/g BERBERIS VULGARIS ROOT BARK;
  • 15 [hp_X]/g BRYONIA ALBA ROOT;
  • 15 [hp_X]/g OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 15 [hp_X]/g LYTTA VESICATORIA;
  • 15 [hp_X]/g CEANOTHUS AMERICANUS LEAF;
  • 15 [hp_X]/g CHELIDONIUM MAJUS;
  • 15 [hp_X]/g CINCHONA OFFICINALIS BARK;
  • 15 [hp_X]/g CHIONANTHUS VIRGINICUS BARK;
  • 15 [hp_X]/g DIOSCOREA VILLOSA TUBER;
  • 15 [hp_X]/g IRIS VERSICOLOR ROOT;
  • 15 [hp_X]/g SODIUM CARBONATE;
  • 15 [hp_X]/g STRYCHNOS NUX-VOMICA SEED;
  • 15 [hp_X]/g PTELEA TRIFOLIATA BARK;
  • 3 [hp_X]/g SILYBUM MARIANUM SEED;
  • 3 [hp_X]/g ECHINACEA, UNSPECIFIED;
  • 3 [hp_X]/g SOLIDAGO VIRGAUREA FLOWERING TOP;
  • 3 [hp_X]/g TARAXACUM OFFICINALE


Administration Route(s): ORAL

Dosage Form(s): PELLET

Pharmacy Class(es):
  • Standardized Chemical Allergen [EPC];
  • Increased Histamine Release [PE];
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Ammonium Ion Binding Activity [MoA];
  • Nitrogen Binding Agent [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Increased Histamine Release [PE];
  • Cell-mediated Immunity [PE];
  • Increased IgG Production [PE];
  • Allergens [CS];
  • Plant Proteins [CS];
  • Seed Storage Proteins [CS]

Labeler Information

Labeler Name: Newton Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/1/2011

Package Information

No. Package Code Package Description Billing Unit
155714-4545-128.35 g in 1 BOTTLE, GLASS (55714-4545-1)
255714-4545-256.7 g in 1 BOTTLE, GLASS (55714-4545-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55714-4545The 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 PRESCRIPTION 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 NAMELymphatic DrainerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAsterias rubens, Aur. met.,Belladonna, Benzoicum acidum, Berber. vulg., Bryonia, Calc. carb., Cantharis, Ceanothus, Chelidonium majus Chionanthus virginica, Cinchona, Dioscorea ,Iris versicolor, Nat. carb., Nux vom., Ptelea, Carduus mar., Echinacea, Solidago, TaraxacumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPELLETThe 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 DATE6/1/2011This 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 NAMENewton Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEASTERIAS RUBENS; GOLD; ATROPA BELLADONNA; BENZOIC ACID; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; LYTTA VESICATORIA; CEANOTHUS AMERICANUS LEAF; CHELIDONIUM MAJUS; CINCHONA OFFICINALIS BARK; CHIONANTHUS VIRGINICUS BARK; DIOSCOREA VILLOSA TUBER; IRIS VERSICOLOR ROOT; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; PTELEA TRIFOLIATA BARK; SILYBUM MARIANUM SEED; ECHINACEA, UNSPECIFIED; SOLIDAGO VIRGAUREA FLOWERING TOP; TARAXACUM OFFICINALEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 3; 3; 3; 3 
ACTIVE INGRED UNIT[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g 
PHARM CLASSESStandardized Chemical Allergen [EPC],Increased Histamine Release [PE],Allergens [CS],Cell-mediated Immunity [PE],Ammonium Ion Binding Activity [MoA],Nitrogen Binding Agent [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Plant Proteins [CS],Seed Storage Proteins [CS] 

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