NDC 69676-0055 Genexa Kids Allergy Care
Allium Cepa,Dulcamara,Euphrasia Officinalis,Nux Vomica,Pulsatilla,Rosa - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 69676-0055?
What are the uses for Genexa Kids Allergy Care?
What are Genexa Kids Allergy Care Active Ingredients?
- BLACK MUSTARD SEED 12 [hp_X]/1
- EUPHRASIA STRICTA 12 [hp_X]/1
- ONION 12 [hp_X]/1 - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
- PULSATILLA PRATENSIS 12 [hp_X]/1
- ROSA DAMASCENA FLOWERING TOP 6 [hp_X]/1
- SCHOENOCAULON OFFICINALE SEED 12 [hp_X]/1
- SOLANUM DULCAMARA STEM 12 [hp_X]/1
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/1
- WYETHIA HELENIOIDES ROOT 12 [hp_X]/1
Which are Genexa Kids Allergy Care UNII Codes?
The UNII codes for the active ingredients in this product are:
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (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 STEM (UNII: IR986LE7DF)
- SOLANUM DULCAMARA STEM (UNII: IR986LE7DF) (Active Moiety)
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- ROSA DAMASCENA FLOWERING TOP (UNII: 21W82Q764G)
- ROSA DAMASCENA FLOWERING TOP (UNII: 21W82Q764G) (Active Moiety)
- BLACK MUSTARD SEED (UNII: 8LTY55LQ8D)
- BLACK MUSTARD SEED (UNII: 8LTY55LQ8D) (Active Moiety)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (Active Moiety)
Which are Genexa Kids 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:
- ACAI (UNII: 46AM2VJ0AW)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- RICE BRAN (UNII: R60QEP13IC)
- DEXTROSE (UNII: IY9XDZ35W2)
Which are the Pharmacologic Classes for Genexa Kids Allergy Care?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
- Vegetable 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".