NDC 11822-0472 Sinus Wash Pre Mixed Ready To Use Rite Aid
Sodium Chloride,Sodium Bicarbonate Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid Corporation
- 11822-0472 - Sinus Wash Pre Mixed Ready To Use
Product Packages
NDC Code 11822-0472-8
Package Description: 1 KIT in 1 KIT * 3 PACKET in 1 KIT / 3000 mg in 1 PACKET * 1 BOTTLE in 1 KIT / 240 mg in 1 BOTTLE
Product Details
What is NDC 11822-0472?
What are the uses for Sinus Wash Pre Mixed Ready To Use Rite Aid?
Which are Sinus Wash Pre Mixed Ready To Use Rite Aid UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
Which are Sinus Wash Pre Mixed Ready To Use Rite Aid 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)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
What is the NDC to RxNorm Crosswalk for Sinus Wash Pre Mixed Ready To Use Rite Aid?
- RxCUI: 1542919 - sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal Solution
- RxCUI: 1542919 - NaHCO3 700 MG / NaCl 2300 MG Powder for Nasal Solution
* 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".