NDC 62106-0623 Hfe
Apis Mellifica,Belladonna,Caulophyllum Thalictroides,Cimicifuga Racemosa,Dioscorea - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62106 - Seroyal Usa
- 62106-0623 - Hfe
Product Packages
NDC Code 62106-0623-0
Package Description: 30 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 62106-0623?
What are the uses for Hfe?
What are Hfe Active Ingredients?
- APIS MELLIFERA 5 [hp_X]/30mL
- ATROPA BELLADONNA 4 [hp_X]/30mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
- BLACK COHOSH 6 [hp_X]/30mL
- CAULOPHYLLUM THALICTROIDES ROOT 4 [hp_X]/30mL
- CHAMAELIRIUM LUTEUM ROOT 4 [hp_X]/30mL
- DIOSCOREA VILLOSA ROOT 4 [hp_X]/30mL
- GELSEMIUM SEMPERVIRENS ROOT 8 [hp_X]/30mL
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 10 [hp_X]/30mL
- ORYCTOLAGUS CUNICULUS ADRENAL GLAND 10 [hp_X]/30mL
- ORYCTOLAGUS CUNICULUS OVARY 10 [hp_X]/30mL
- ORYCTOLAGUS CUNICULUS UTERUS 10 [hp_X]/30mL
- VIBURNUM OPULUS BARK 2 [hp_X]/30mL
Which are Hfe UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8)
- DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8) (Active Moiety)
- ORYCTOLAGUS CUNICULUS UTERUS (UNII: NQX84Z32G6)
- ORYCTOLAGUS CUNICULUS UTERUS (UNII: NQX84Z32G6) (Active Moiety)
- ORYCTOLAGUS CUNICULUS OVARY (UNII: XA09528U2R)
- ORYCTOLAGUS CUNICULUS OVARY (UNII: XA09528U2R) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH)
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH) (Active Moiety)
- CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U)
- CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U) (Active Moiety)
- ORYCTOLAGUS CUNICULUS ADRENAL GLAND (UNII: QGY289M89Q)
- ORYCTOLAGUS CUNICULUS ADRENAL GLAND (UNII: QGY289M89Q) (Active Moiety)
- VIBURNUM OPULUS BARK (UNII: T1UG6H6805)
- VIBURNUM OPULUS BARK (UNII: T1UG6H6805) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
Which are Hfe 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 Hfe?
- Allergens - [CS]
- Bee Venoms - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
* 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".