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  4. NDC Product Code: 57955-0298 Influenza Multi-strain Flu Medicine

NDC 57955-0298 Influenza Multi-strain Flu Medicine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57955-0298?
  4. Influenza Multi-strain Flu Medicine Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
57955-0298
Proprietary Name:
Influenza Multi-strain Flu Medicine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
King Bio Inc.
Labeler Code:
57955
Product Label ID:
e5ecfc11-d8e1-4341-bccb-a705a24dc771
Start Marketing Date: [9]
01-22-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 57955-0298?

The NDC code 57955-0298 is assigned by the FDA to the product Influenza Multi-strain Flu Medicine 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 57955-0298-2 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 Influenza Multi-strain Flu Medicine?

Initially, depress pump until primed. Spray one dose directly into mouth.Adults 12 and up: 3 sprays 3 times per day.Children 2-12: 2 sprays 3 times per day.Children 2mo-2yr.: 1 spray 3 times per day.

Which are Influenza Multi-strain Flu Medicine UNII Codes?

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

Which are Influenza Multi-strain Flu Medicine 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".