NDC 69842-765-02 Fluticasone Propionate

Fluticasone Propionate

NDC Package Code 69842-765-02

The NDC Code 69842-765-02 is assigned to a package of 2 bottle, spray in 1 carton > 120 spray, metered in 1 bottle, spray of Fluticasone Propionate, a human over the counter drug labeled by Cvs Pharmacy. The product's dosage form is spray, metered and is administered via nasal form.

Field Name Field Value
NDC Code 69842-765-02
Package Description 2 BOTTLE, SPRAY in 1 CARTON > 120 SPRAY, METERED in 1 BOTTLE, SPRAY
Proprietary Name Fluticasone Propionate What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Fluticasone Propionate 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.
Drug Uses Fluticasone is used to relieve seasonal and year-round allergic and non-allergic nasal symptoms, such as stuffy/runny nose, itching, and sneezing. It can also help relieve allergy eye symptoms such as itchy, watery eyes. This medication belongs to a class of drugs known as corticosteroids. It works in your nose to block the effects of substances that cause allergies (such as pollen, pet dander, dust mites, mold) and to reduce swelling.
11-Digit NDC Billing Format 69842076502 NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
Product Type Human Otc Drug 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.
Labeler Name Cvs Pharmacy
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)
  • Nasal - Administration to the nose; administered by way of the nose.
  • Nasal - Administration to the nose; administered by way of the nose.
Active Ingredient(s)
  • FLUTICASONE PROPIONATE 50 ug/1
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Marketing Category ANDA - A product marketed under an approved Abbreviated New Drug Application. 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.
FDA Application Number ANDA208150 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.
Start Marketing Date 09-12-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date 12-31-2020 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.
Exclude Flag N 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. Values = ‘Y’ or ‘N’.

NDC Code Structure

  • 69842 - Cvs Pharmacy
    • 69842-765 - Fluticasone Propionate
      • 69842-765-02 - 2 BOTTLE, SPRAY in 1 CARTON

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Other Product Packages

The following packages are also available for Fluticasone Propionate with product NDC 69842-765.

NDC Package CodePackage Description
69842-765-011 BOTTLE, SPRAY in 1 CARTON > 120 SPRAY, METERED in 1 BOTTLE, SPRAY
69842-765-033 BOTTLE, SPRAY in 1 CARTON > 120 SPRAY, METERED in 1 BOTTLE, SPRAY
69842-765-041 BOTTLE, SPRAY in 1 CARTON > 60 SPRAY, METERED in 1 BOTTLE, SPRAY

* Please review the disclaimer below.