1. Home
  2. Labeler Index
  3. Kroger Company
  4. NDC Product Code: 30142-443 24 Hour Nasal Allergy

NDC 30142-443 24 Hour Nasal Allergy

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 30142-443?
  5. 24 Hour Nasal Allergy Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
30142-443
Proprietary Name:
24 Hour Nasal Allergy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kroger Company
Labeler Code:
30142
Product Label ID:
8601b678-f5bd-427d-a468-4f3c6f097929
Start Marketing Date: [9]
04-10-2016
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - OFF WHITE)

Code Structure Chart

Product Details

What is NDC 30142-443?

The NDC code 30142-443 is assigned by the FDA to the product 24 Hour Nasal Allergy which is product labeled by Kroger Company. The product's dosage form is . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for 24 Hour Nasal Allergy?

Read insert (inside package) on how to:•get a new bottle ready (primed) before first use•prime bottle again if not used for more than 2 weeks•use the spray•clean the spray nozzleADULTS AND CHILDREN 12 YEARS OF AGE AND OLDERadults and children 12 years of age and older•once daily, spray 2 times into each nostril while sniffing gently•once your allergy symptoms improve, reduce to 1 spray in each nostril per dayCHILDREN 2 TO UNDER 12 YEARS OF AGE•the growth rate of some children may be slower while using this product. Talk to your child’s doctor if your child needs to use the spray for longer than two months a year.children 6 to under 12 years of age•an adult should supervise use•once daily, spray 1 time into each nostril while sniffing gently•if allergy symptoms do not improve, increase to 2 sprays in each nostril per day. Once allergy symptoms improve, reduce to 1 spray in each nostril per day.children 2 to under 6 years of age•an adult should supervise use•once daily, spray 1 time into each nostril while sniffing gentlychildren under 2 years of age•do not use•do not use more than directed•if you forget a dose, do not double the next dose•do not spray into eyes or mouth•if allergy symptoms do not improve after one week, stop using and talk to a doctor•do not use for the common cold•shake well before each use

Which are 24 Hour Nasal Allergy UNII Codes?

The UNII codes for the active ingredients in this product are:

  • TRIAMCINOLONE ACETONIDE (UNII: F446C597KA)
  • TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (Active Moiety)

Which are 24 Hour Nasal Allergy 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:

What is the NDC to RxNorm Crosswalk for 24 Hour Nasal Allergy?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1797913 - triamcinolone acetonide 55 MCG/ACTUAT Metered Dose Nasal Spray
  • RxCUI: 1797913 - triamcinolone acetonide 0.055 MG/ACTUAT Metered Dose Nasal Spray

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[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".