83027-0146 NDC - FEMALE LIQUESCENCE (DIOSCOREA VILLOSA, GLYCYRRHIZA GLABRA, HAMAMELIS VIRGINIANA, RUBUS IDAEUS, VIBURNUM OPULUS, CAULOPHYLLUM THALICTROIDES, ESTRADIOL, OOPHORINUM (SUIS), PROGESTERONE, UTERUS (SUIS), HUMAN GROWTH HORMONE (HGH), IGNATIA AMARA)

Drug Information

  • Product NDC: 83027-0146
  • Proprietary Name: Female Liquescence
  • Non Proprietary Name: Dioscorea Villosa, Glycyrrhiza Glabra, Hamamelis Virginiana, Rubus Idaeus, Viburnum Opulus, Caulophyllum Thalictroides, Estradiol, Oophorinum (Suis), Progesterone, Uterus (Suis), Human Growth Hormone (HGH), Ignatia Amara
  • Active Ingredient(s): 3 [hp_X]/mL CAULOPHYLLUM THALICTROIDES ROOT; 2 [hp_X]/mL DIOSCOREA VILLOSA TUBER; 6 [hp_X]/mL ESTRADIOL; 2 [hp_X]/mL GLYCYRRHIZA GLABRA; 2 [hp_X]/mL HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; 6 [hp_X]/mL PROGESTERONE; 2 [hp_X]/mL RUBUS IDAEUS LEAF; 12 [hp_X]/mL SOMATROPIN; 12 [hp_X]/mL STRYCHNOS IGNATII SEED; 6 [hp_X]/mL SUS SCROFA OVARY; 6 [hp_X]/mL SUS SCROFA UTERUS; 2 [hp_X]/mL VIBURNUM OPULUS BARK
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Estradiol Congeners [CS]; Estrogen Receptor Agonists [MoA]; Estrogen [EPC]; Human Growth Hormone [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Progesterone [CS]; Progesterone [EPC]; Recombinant Human Growth Hormone [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Nutritional Specialties, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/25/2024

Package Information

No. Package Code Package Description Billing Unit
183027-0146-1120 mL in 1 BOTTLE, GLASS (83027-0146-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC83027-0146The 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 NAMEFemale LiquescenceThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEDioscorea Villosa, Glycyrrhiza Glabra, Hamamelis Virginiana, Rubus Idaeus, Viburnum Opulus, Caulophyllum Thalictroides, Estradiol, Oophorinum (Suis), Progesterone, Uterus (Suis), Human Growth Hormone (HGH), Ignatia AmaraThe 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 DATE9/25/2024This 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 NAMENutritional Specialties, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECAULOPHYLLUM THALICTROIDES ROOT; DIOSCOREA VILLOSA TUBER; ESTRADIOL; GLYCYRRHIZA GLABRA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; PROGESTERONE; RUBUS IDAEUS LEAF; SOMATROPIN; STRYCHNOS IGNATII SEED; SUS SCROFA OVARY; SUS SCROFA UTERUS; VIBURNUM OPULUS BARKAn 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 STRENGTH3; 2; 6; 2; 2; 6; 2; 12; 12; 6; 6; 2 
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 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Human Growth Hormone [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Progesterone [CS], Progesterone [EPC], Recombinant Human Growth Hormone [EPC] 

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This page was last updated on: 12/19/2025

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