43857-0304 NDC - LYMPH (ECHINACEA (ANGUSTIFOLIA), PHYTOLACCA DECANDRA, COLLINSONIA CANADENSIS, KALI IODATUM, PINUS SYLVESTRIS, PIX LIQUIDA, FERRUM PHOSPHORICUM, AESCULUS HIPPOCASTANUM, BARYTA CARBONICA, BERBERIS VULGARIS, BUFO RANA, CALCAREA CARBONICA, CAUSTICUM, HEPAR SULPHURIS CALCAREUM, KREOSOTUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, NITRICUM ACIDUM, PHOSPHORUS, PULSATILLA (VULGARIS), SILICEA, STELLARIA MEDIA, SULPHUR, TEREBINTHINA, THUJA OCCIDENTALIS)

Drug Information

Product NDC: 43857-0304

Proprietary Name: Lymph

Non Proprietary Name: Echinacea (Angustifolia), Phytolacca Decandra, Collinsonia Canadensis, Kali Iodatum, Pinus Sylvestris, Pix Liquida, Ferrum Phosphoricum, Aesculus Hippocastanum, Baryta Carbonica, Berberis Vulgaris, Bufo Rana, Calcarea Carbonica, Causticum, Hepar Sulphuris Calcareum, Kreosotum, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Nitricum Acidum, Phosphorus, Pulsatilla (Vulgaris), Silicea, Stellaria Media, Sulphur, Terebinthina, Thuja Occidentalis

Active Ingredient(s):
  • 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA;
  • 3 [hp_X]/mL PHYTOLACCA AMERICANA ROOT;
  • 3 [hp_X]/mL COLLINSONIA CANADENSIS ROOT;
  • 6 [hp_X]/mL POTASSIUM IODIDE;
  • 6 [hp_X]/mL PINUS SYLVESTRIS LEAFY TWIG;
  • 6 [hp_X]/mL PINE TAR;
  • 8 [hp_X]/mL FERROSOFERRIC PHOSPHATE;
  • 12 [hp_X]/mL HORSE CHESTNUT;
  • 12 [hp_X]/mL BARIUM CARBONATE;
  • 12 [hp_X]/mL BERBERIS VULGARIS ROOT BARK;
  • 12 [hp_X]/mL BUFO BUFO CUTANEOUS GLAND;
  • 12 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 12 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE;
  • 12 [hp_X]/mL CAUSTICUM;
  • 12 [hp_X]/mL CALCIUM SULFIDE;
  • 12 [hp_X]/mL WOOD CREOSOTE;
  • 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE;
  • 12 [hp_X]/mL MERCURIUS SOLUBILIS;
  • 12 [hp_X]/mL SODIUM CHLORIDE;
  • 12 [hp_X]/mL NITRIC ACID;
  • 12 [hp_X]/mL PHOSPHORUS;
  • 12 [hp_X]/mL PULSATILLA VULGARIS;
  • 12 [hp_X]/mL SILICON DIOXIDE;
  • 12 [hp_X]/mL STELLARIA MEDIA;
  • 12 [hp_X]/mL SULFUR;
  • 12 [hp_X]/mL TURPENTINE OIL;
  • 12 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: BioActive Nutritional, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/21/2014
End Marketing Date:2/9/2021

Package Information

No. Package Code Package Description Billing Unit
143857-0304-160 mL in 1 BOTTLE, DROPPER (43857-0304-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43857-0304The 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 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 NAMEEchinacea (Angustifolia), Phytolacca Decandra, Collinsonia Canadensis, Kali Iodatum, Pinus Sylvestris, Pix Liquida, Ferrum Phosphoricum, Aesculus Hippocastanum, Baryta Carbonica, Berberis Vulgaris, Bufo Rana, Calcarea Carbonica, Causticum, Hepar Sulphuris Calcareum, Kreosotum, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Nitricum Acidum, Phosphorus, Pulsatilla (Vulgaris), Silicea, Stellaria Media, Sulphur, Terebinthina, Thuja OccidentalisThe 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 DATE6/21/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE2/9/2021This 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 NAMEBioActive Nutritional, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEECHINACEA ANGUSTIFOLIA; PHYTOLACCA AMERICANA ROOT; COLLINSONIA CANADENSIS ROOT; POTASSIUM IODIDE; PINUS SYLVESTRIS LEAFY TWIG; PINE TAR; FERROSOFERRIC PHOSPHATE; HORSE CHESTNUT; BARIUM CARBONATE; BERBERIS VULGARIS ROOT BARK; BUFO BUFO CUTANEOUS GLAND; OYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; CAUSTICUM; CALCIUM SULFIDE; WOOD CREOSOTE; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; SODIUM CHLORIDE; NITRIC ACID; PHOSPHORUS; PULSATILLA VULGARIS; SILICON DIOXIDE; STELLARIA MEDIA; SULFUR; TURPENTINE OIL; THUJA OCCIDENTALIS LEAFY TWIGThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH3; 3; 3; 6; 6; 6; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 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 

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