NDC 83027-0018 Female Liquescence
Dioscorea Villosa,Glycyrrhiza Glabra,Hamamelis Virginiana,Rubus Idaeus,Viburnum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 83027 - Nutritional Specialties, Inc.
- 83027-0018 - Female Liquescence
Product Packages
NDC Code 83027-0018-1
Package Description: 120 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 83027-0018?
What are the uses for Female Liquescence?
What are Female Liquescence Active Ingredients?
- CAULOPHYLLUM THALICTROIDES ROOT 3 [hp_X]/mL
- DIOSCOREA VILLOSA TUBER 2 [hp_X]/mL
- GLYCYRRHIZA GLABRA 2 [hp_X]/mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 2 [hp_X]/mL
- RUBUS IDAEUS LEAF 2 [hp_X]/mL
- SOMATROPIN 12 [hp_X]/mL - A 191-amino acid polypeptide hormone secreted by the human adenohypophysis (PITUITARY GLAND, ANTERIOR), also known as GH or somatotropin. Synthetic growth hormone, termed somatropin, has replaced the natural form in therapeutic usage such as treatment of dwarfism in children with growth hormone deficiency.
- STRYCHNOS IGNATII SEED 12 [hp_X]/mL
- SUS SCROFA OVARY 6 [hp_X]/mL
- SUS SCROFA UTERUS 6 [hp_X]/mL
- VIBURNUM OPULUS BARK 2 [hp_X]/mL
Which are Female Liquescence UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)
- DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8) (Active Moiety)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- RUBUS IDAEUS LEAF (UNII: 8O2V33JG64)
- RUBUS IDAEUS LEAF (UNII: 8O2V33JG64) (Active Moiety)
- VIBURNUM OPULUS BARK (UNII: T1UG6H6805)
- VIBURNUM OPULUS BARK (UNII: T1UG6H6805) (Active Moiety)
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH)
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH) (Active Moiety)
- SUS SCROFA OVARY (UNII: S7YTV04R8O)
- SUS SCROFA OVARY (UNII: S7YTV04R8O) (Active Moiety)
- SUS SCROFA UTERUS (UNII: 2595C75F1P)
- SUS SCROFA UTERUS (UNII: 2595C75F1P) (Active Moiety)
- SOMATROPIN (UNII: NQX9KB6PCL)
- SOMATROPIN (UNII: NQX9KB6PCL) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
Which are Female Liquescence Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Female Liquescence?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Human Growth Hormone - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Recombinant Human Growth Hormone - [EPC] (Established Pharmacologic Class)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An 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.
[3] What kind of product is this? - Indicates 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product 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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".