64616-090 NDC - FEM REPAIR NON-PREG (FEM GLANDULAR AND TISSUE AID)

Drug Information

Product NDC: 64616-090

Proprietary Name: Fem Repair Non-Preg

Non Proprietary Name: Fem Glandular and Tissue Aid

Active Ingredient(s):
  • 14 [hp_X]/mL ANTIMONY ARSENATE;
  • 6 [hp_X]/mL CENTELLA ASIATICA;
  • 6 [hp_X]/mL CHIONANTHUS VIRGINICUS BARK;
  • 6 [hp_X]/mL CHRYSOPOGON ZIZANIOIDES ROOT;
  • 7 [hp_X]/mL CLAVICEPS PURPUREA SCLEROTIUM;
  • 15 [hp_X]/mL DAPHNE MEZEREUM BARK;
  • 6 [hp_X]/mL GENTIANA LUTEA ROOT;
  • 12 [hp_X]/mL MERCURIUS SOLUBILIS;
  • 10 [hp_X]/mL OXALIC ACID DIHYDRATE;
  • 20 [hp_X]/mL POTASSIUM PHOSPHATE, DIBASIC;
  • 6 [hp_X]/mL RUTA GRAVEOLENS FLOWERING TOP;
  • 20 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP;
  • 6 [hp_C]/mL SUS SCROFA PITUITARY GLAND;
  • 6 [hp_X]/mL VALERIANA OFFICINALIS WHOLE;
  • 15 [hp_X]/mL ZINC OXIDE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Copper Absorption Inhibitor [EPC];
  • Decreased Copper Ion Absorption [PE]

Labeler Information

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

Package Information

No. Package Code Package Description Billing Unit
164616-090-0259 mL in 1 BOTTLE, DROPPER (64616-090-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64616-090The 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 NAMEFem Repair Non-PregThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEFem Glandular and Tissue AidThe 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, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEANTIMONY ARSENATE; CENTELLA ASIATICA; CHIONANTHUS VIRGINICUS BARK; CHRYSOPOGON ZIZANIOIDES ROOT; CLAVICEPS PURPUREA SCLEROTIUM; DAPHNE MEZEREUM BARK; GENTIANA LUTEA ROOT; MERCURIUS SOLUBILIS; OXALIC ACID DIHYDRATE; POTASSIUM PHOSPHATE, DIBASIC; RUTA GRAVEOLENS FLOWERING TOP; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA PITUITARY GLAND; VALERIANA OFFICINALIS WHOLE; ZINC OXIDEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH14; 6; 6; 6; 7; 15; 6; 12; 10; 20; 6; 20; 6; 6; 15 
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_C]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESCopper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] 

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This page was last updated on: 2/1/2023