NDC 43857-0165 Gynetox
Angelica Archangelica,Cimicifuga Racemosa,Zincum Gluconicum,Funiculus Umbilicalis - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43857-0165?
What are the uses for Gynetox?
What are Gynetox Active Ingredients?
- ANEMONE PULSATILLA 12 [hp_X]/mL
- ANGELICA ARCHANGELICA ROOT 3 [hp_X]/mL
- BLACK COHOSH 3 [hp_X]/mL
- BORIC ACID 12 [hp_X]/mL
- CANDIDA ALBICANS 30 [hp_X]/mL - A unicellular budding fungus which is the principal pathogenic species causing CANDIDIASIS (moniliasis).
- HUMAN HERPESVIRUS 1 30 [hp_X]/mL - The type species of SIMPLEXVIRUS causing most forms of non-genital herpes simplex in humans. Primary infection occurs mainly in infants and young children and then the virus becomes latent in the dorsal root ganglion. It then is periodically reactivated throughout life causing mostly benign conditions.
- HUMAN HERPESVIRUS 2 30 [hp_X]/mL
- HUMAN PAPILLOMAVIRUS 30 [hp_X]/mL
- JUNIPERUS SABINA LEAFY TWIG 30 [hp_X]/mL
- MERCURIUS SOLUBILIS 12 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL
- PHOSPHORUS 30 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
- SUS SCROFA ADRENAL GLAND 9 [hp_X]/mL
- SUS SCROFA LYMPH 8 [hp_X]/mL
- SUS SCROFA OVARY 8 [hp_X]/mL
- SUS SCROFA THYROID 9 [hp_X]/mL
- SUS SCROFA UMBILICAL CORD 8 [hp_X]/mL
- SUS SCROFA UTERUS 8 [hp_X]/mL
- WOOD CREOSOTE 12 [hp_X]/mL
- ZINC GLUCONATE 6 [hp_X]/mL
Which are Gynetox UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN)
- ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H)
- SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (Active Moiety)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L) (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)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
- BORIC ACID (UNII: R57ZHV85D4)
- BORIC ACID (UNII: R57ZHV85D4) (Active Moiety)
- WOOD CREOSOTE (UNII: 3JYG22FD73)
- WOOD CREOSOTE (UNII: 3JYG22FD73) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- JUNIPERUS SABINA LEAFY TWIG (UNII: Z5BEX9K2G1)
- JUNIPERUS SABINA LEAFY TWIG (UNII: Z5BEX9K2G1) (Active Moiety)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC) (Active Moiety)
- HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL)
- HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL) (Active Moiety)
- HUMAN HERPESVIRUS 2 (UNII: 74J6DNH49U)
- HUMAN HERPESVIRUS 2 (UNII: 74J6DNH49U) (Active Moiety)
- HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J)
- HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J) (Active Moiety)
Which are Gynetox 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 Gynetox?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
- Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
- Fungal Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Fungal Allergenic Extract - [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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".