NDC 69676-0052 Genexa Allergy Care
Allium Cepa,Ambrosia Artemisiifolia,Arundo Mauritanica,Dulcamara,Euphrasia Officinalis,Nux - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69676 - Genexa Inc.
- 69676-0052 - Genexa Allergy Care
Product Characteristics
Product Packages
NDC Code 69676-0052-1
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
NDC Code 69676-0052-3
Package Description: 2 TABLET, CHEWABLE in 1 POUCH
Product Details
What is NDC 69676-0052?
What are the uses for Genexa Allergy Care?
What are Genexa Allergy Care Active Ingredients?
- ALLIUM CEPA WHOLE 12 [hp_X]/1
- AMBROSIA ARTEMISIIFOLIA 12 [hp_X]/1
- ARUNDO PLINIANA ROOT 12 [hp_X]/1
- BLACK MUSTARD SEED 12 [hp_X]/1
- EUPHRASIA STRICTA 12 [hp_X]/1
- LOBARIA PULMONARIA 12 [hp_X]/1
- PULSATILLA PRATENSIS 12 [hp_X]/1
- RANUNCULUS BULBOSUS WHOLE 12 [hp_X]/1
- SCHOENOCAULON OFFICINALE SEED 12 [hp_X]/1
- SOLANUM DULCAMARA TOP 12 [hp_X]/1
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/1
- WYETHIA HELENIOIDES ROOT 12 [hp_X]/1
Which are Genexa Allergy Care UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- BLACK MUSTARD SEED (UNII: 8LTY55LQ8D)
- BLACK MUSTARD SEED (UNII: 8LTY55LQ8D) (Active Moiety)
- LOBARIA PULMONARIA (UNII: D1YM0P5Z2T)
- LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (Active Moiety)
- ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC)
- ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC) (Active Moiety)
- RANUNCULUS BULBOSUS WHOLE (UNII: AEQ8NXJ0MB)
- RANUNCULUS BULBOSUS WHOLE (UNII: AEQ8NXJ0MB) (Active Moiety)
- PULSATILLA PRATENSIS (UNII: 8E272251DI)
- PULSATILLA PRATENSIS (UNII: 8E272251DI) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- SOLANUM DULCAMARA TOP (UNII: KPS1B1162N)
- SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (Active Moiety)
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (Active Moiety)
- ALLIUM CEPA WHOLE (UNII: 8P2VLG2456)
- ALLIUM CEPA WHOLE (UNII: 8P2VLG2456) (Active Moiety)
Which are Genexa Allergy Care 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:
- RICE BRAN (UNII: R60QEP13IC)
- DEXTROSE (UNII: IY9XDZ35W2)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
Which are the Pharmacologic Classes for Genexa Allergy Care?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
* 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".