NDC 82506-100 Prevencia

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82506-100
Proprietary Name:
Prevencia
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Core Consumer Healthcare Llc
Labeler Code:
82506
Start Marketing Date: [9]
10-17-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 82506-100-15

Package Description: 15 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 82506-100?

The NDC code 82506-100 is assigned by the FDA to the product Prevencia which is product labeled by Core Consumer Healthcare Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82506-100-15 15 ml 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 Prevencia?

DirectionsAdults and children 12 years of age and older:Shake well before using. Remove cap and clip. Before using for the first time, prime pump by depressing the rim a few times for the fine mist to appear. Without tilting head, place tip of nozzle in the nostril. Without inhaling, depress the rim and pump once into each nostril. Do not overspray. Wipe away any excess. Use every 4 to 6 hours.

Which are Prevencia UNII Codes?

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

Which are Prevencia 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:

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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".