NDC 32267-940 Gy-na-tren
Boric Acid,Marigold,Coneflower,Arborvitae,Borate Of Sodium,Beechwood Kreosote,Wind - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 32267-940?
What are the uses for Gy-na-tren?
Which are Gy-na-tren UNII Codes?
The UNII codes for the active ingredients in this product are:
- LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5)
- LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- BORIC ACID (UNII: R57ZHV85D4)
- BORIC ACID (UNII: R57ZHV85D4) (Active Moiety)
- WOOD CREOSOTE (UNII: 3JYG22FD73)
- WOOD CREOSOTE (UNII: 3JYG22FD73) (Active Moiety)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- BORATE ION (UNII: 44OAE30D22) (Active Moiety)
- PULSATILLA PRATENSIS (UNII: 8E272251DI)
- PULSATILLA PRATENSIS (UNII: 8E272251DI) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
Which are Gy-na-tren 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:
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- LEUCINE (UNII: GMW67QNF9C)
- POTATO (UNII: CFE1S8DYWD)
- CHICKPEA (UNII: N91637DNW9)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- GELATIN (UNII: 2G86QN327L)
- COCONUT OIL (UNII: Q9L0O73W7L)
- SODIUM ASCORBATE (UNII: S033EH8359)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
* 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.
[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.
[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".