NDC 57955-5134 Sinus Relief

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:
Proprietary Name:
Sinus Relief
Product Type: [3]
Labeler Name: [5]
King Bio Inc
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Packages

NDC Code 57955-5134-2

Package Description: 1 BOTTLE, SPRAY in 1 BOX / 59 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 57955-5134?

The NDC code 57955-5134 is assigned by the FDA to the product Sinus Relief which is product labeled by King Bio Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57955-5134-2 1 bottle, spray in 1 box / 59 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 Sinus Relief?

Uses temporarily relieves symptoms due to sinus discomforts associated with inflamed sinuses, hay fever or upper respiratory allergies:sinus pain and pressurerunny nosesinus headachessore throat nasal congestiondry mucus membranessneezingitchy, burning eyesReference image sinus.jpg

Which are Sinus Relief UNII Codes?

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

Which are Sinus Relief 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".