24 Hour Nasal Allergy
NDC 30142-443

View dosage, usage, ingredients, routes, and UNII mappings.
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
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

24 Hour Nasal Allergy is a ANDA-approved product labeled by Kroger Company. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a white product. This product entry covers the primary NDC 30142-443 and 2 associated package configurations. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
30142-443
Proprietary Name:
24 Hour Nasal Allergy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Kroger Company
Labeler Code:
30142
Product Label ID:
8601b678-f5bd-427d-a468-4f3c6f097929
FDA Application Number: [6]
ANDA078104
Marketing Category: [8]
ANDA - A product marketed under an approved Abbreviated New Drug Application.

Marketing Timeline

Start Marketing Date: [9]
04-10-2016
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I

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. This pharmaceutical product is labeled by Kroger Company and is currently categorized as listed product. In terms of distribution, this product is available in 2 different package configurations. The associated package NDC(s) include: 30142-443-01, 30142-443-03. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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 the associated 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 the Inactive Ingredients associated 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 this product?

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 full disclaimer at the bottom of this page.

Patient Education

Triamcinolone Nasal Spray


Triamcinolone nasal spray is used to relieve sneezing, runny, stuffy, or itchy nose and itchy, watery eyes caused by hay fever or other allergies. Triamcinolone nasal spray should not be used to treat symptoms (e.g., sneezing, stuffy, runny, or itchy nose) caused by the common cold. Triamcinolone is in a class of medications called corticosteroids. It works by blocking the release of certain natural substances that cause allergy symptoms.
[Learn More]


Steroids


You may have heard of anabolic steroids, which can have harmful effects. But there's another type of steroid - sometimes called a corticosteroid - that treats a variety of problems. These steroids are similar to hormones that your adrenal glands make to fight stress associated with illnesses and injuries. They reduce inflammation and affect the immune system.

You may need to take corticosteroids to treat:

  • Arthritis
  • Asthma
  • Autoimmune diseases such as lupus and multiple sclerosis
  • Skin conditions such as eczema and rashes
  • Some kinds of cancer

Steroids are strong medicines, and they can have side effects, including weakened bones and cataracts. Because of this, you usually take them for as short a time as possible.


[Learn More]


* Please review the full disclaimer at the bottom of this page.

Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the FDA Application Number? This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".