NDC 41167-5800 Nasacort Allergy 24hr

Triamcinolone Acetonide Spray, Metered Nasal - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
41167-5800
Proprietary Name:
Nasacort Allergy 24hr
Non-Proprietary Name: [1]
Triamcinolone Acetonide
Substance Name: [2]
Triamcinolone Acetonide
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray, Metered - A non-pressurized dosage form consisting of valves which allow the dispensing of a specified quantity of spray upon each activation.
Administration Route(s): [4]
  • Nasal - Administration to the nose; administered by way of the nose.
  • Labeler Name: [5]
    Chattem, Inc.
    Labeler Code:
    41167
    FDA Application Number: [6]
    NDA020468
    Marketing Category: [8]
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date: [9]
    02-03-2014
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Packages

    NDC Code 41167-5800-1

    Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 30 SPRAY, METERED in 1 BOTTLE, SPRAY

    NDC Code 41167-5800-2

    Package Description: 2 BOTTLE, SPRAY in 1 CARTON / 120 SPRAY, METERED in 1 BOTTLE, SPRAY

    NDC Code 41167-5800-3

    Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 60 SPRAY, METERED in 1 BOTTLE, SPRAY

    NDC Code 41167-5800-5

    Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 120 SPRAY, METERED in 1 BOTTLE, SPRAY

    NDC Code 41167-5800-6

    Package Description: 4 BOTTLE, SPRAY in 1 CARTON / 120 SPRAY, METERED in 1 BOTTLE, SPRAY

    Product Details

    What is NDC 41167-5800?

    The NDC code 41167-5800 is assigned by the FDA to the product Nasacort Allergy 24hr which is a human over the counter drug product labeled by Chattem, Inc.. The generic name of Nasacort Allergy 24hr is triamcinolone acetonide. The product's dosage form is spray, metered and is administered via nasal form. The product is distributed in 5 packages with assigned NDC codes 41167-5800-1 1 bottle, spray in 1 carton / 30 spray, metered in 1 bottle, spray, 41167-5800-2 2 bottle, spray in 1 carton / 120 spray, metered in 1 bottle, spray, 41167-5800-3 1 bottle, spray in 1 carton / 60 spray, metered in 1 bottle, spray, 41167-5800-5 1 bottle, spray in 1 carton / 120 spray, metered in 1 bottle, spray, 41167-5800-6 4 bottle, spray in 1 carton / 120 spray, metered in 1 bottle, spray. 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 Nasacort Allergy 24hr?

    This medication is used in a variety of conditions such as allergic disorders, arthritis, gout, blood diseases, breathing problems, certain cancers, eye diseases, intestinal disorders, collagen and skin diseases. Talk to your doctor about the risks and benefits of triamcinolone, especially if it is to be injected near your spine (epidural). Rare but serious side effects may occur with epidural use. Triamcinolone is known as a corticosteroid hormone (glucocorticoid). It works by decreasing your body's immune response to these diseases and reduces symptoms such as swelling.

    What are Nasacort Allergy 24hr Active Ingredients?

    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.
    • TRIAMCINOLONE ACETONIDE 55 ug/1 - An esterified form of TRIAMCINOLONE. It is an anti-inflammatory glucocorticoid used topically in the treatment of various skin disorders. Intralesional, intramuscular, and intra-articular injections are also administered under certain conditions.

    Which are Nasacort Allergy 24hr 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 Nasacort Allergy 24hr 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 Nasacort Allergy 24hr?

    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
    • RxCUI: 1797915 - Nasacort 55 MCG/ACTUAT Metered Dose Nasal Spray
    • RxCUI: 1797915 - triamcinolone acetonide 0.055 MG/ACTUAT Metered Dose Nasal Spray [Nasacort]
    • RxCUI: 1797915 - Nasacort 0.055 MG/ACTUAT Metered Dose Nasal Spray

    Which are the Pharmacologic Classes for Nasacort Allergy 24hr?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    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 disclaimer below.

    Product Footnotes

    [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.

    [6] 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.

    [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".