64616-097 NDC - LV-FX (LIVER ASSIT)

Drug Information

Product NDC: 64616-097

Proprietary Name: LV-FX

Non Proprietary Name: Liver Assit

Active Ingredient(s):
  • 10 [hp_X]/mL HORSE CHESTNUT;
  • 14 [hp_X]/mL ANACARDIUM OCCIDENTALE FRUIT;
  • 10 [hp_X]/mL ARALIA RACEMOSA ROOT;
  • 15 [hp_X]/mL ARSENIC TRIOXIDE;
  • 15 [hp_X]/mL ARSENIC TRIIODIDE;
  • 7 [hp_X]/mL BELLIS PERENNIS;
  • 20 [hp_X]/mL CALCIUM FLUORIDE;
  • 15 [hp_X]/mL MILK THISTLE;
  • 9 [hp_X]/mL SIMABA CEDRON SEED;
  • 10 [hp_X]/mL CHAMAELIRIUM LUTEUM ROOT;
  • 20 [hp_X]/mL LEDUM PALUSTRE TWIG;
  • 20 [hp_X]/mL MANGANESE ACETATE TETRAHYDRATE;
  • 6 [hp_X]/mL MYRTUS COMMUNIS TOP;
  • 7 [hp_X]/mL PHYSALIS ALKEKENGI FRUIT;
  • 10 [hp_X]/mL RUTA GRAVEOLENS FLOWERING TOP;
  • 30 [hp_X]/mL SELENIUM;
  • 14 [hp_X]/mL FERULA SUMBUL ROOT;
  • 6 [hp_C]/mL THYROID, UNSPECIFIED;
  • 6 [hp_X]/mL VERATRUM VIRIDE ROOT


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: Vitality Works, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:4/8/2013

Package Information

No. Package Code Package Description Billing Unit
164616-097-0259 mL in 1 BOTTLE, DROPPER (64616-097-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64616-097The 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 NAMELV-FXThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMELiver AssitThe 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 DATE4/8/2013This 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 NAMEVitality Works, IncName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEHORSE CHESTNUT; ANACARDIUM OCCIDENTALE FRUIT; ARALIA RACEMOSA ROOT; ARSENIC TRIOXIDE; ARSENIC TRIIODIDE; BELLIS PERENNIS; CALCIUM FLUORIDE; MILK THISTLE; SIMABA CEDRON SEED; CHAMAELIRIUM LUTEUM ROOT; LEDUM PALUSTRE TWIG; MANGANESE ACETATE TETRAHYDRATE; MYRTUS COMMUNIS TOP; PHYSALIS ALKEKENGI FRUIT; RUTA GRAVEOLENS FLOWERING TOP; SELENIUM; FERULA SUMBUL ROOT; THYROID, UNSPECIFIED; VERATRUM VIRIDE ROOTThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH10; 14; 10; 15; 15; 7; 20; 15; 9; 10; 20; 20; 6; 7; 10; 30; 14; 6; 6 
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_C]/mL; [hp_X]/mL 

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This page was last updated on: 10/30/2020