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  4. NDC Product Code: 0220-9316 Rhinallergy Kids

NDC 0220-9316 Rhinallergy Kids

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0220-9316?
  5. Rhinallergy Kids Uses
  6. Active Ingredients UNII Codes
  7. 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:
0220-9316
Proprietary Name:
Rhinallergy Kids
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Boiron
Labeler Code:
0220
Product Label ID:
6dd8e07c-44e2-d89f-e053-2991aa0a5eb7
Start Marketing Date: [9]
06-15-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
9 MM
Imprint(s):
BOIRON
Score:
1

Code Structure Chart

Product Details

What is NDC 0220-9316?

The NDC code 0220-9316 is assigned by the FDA to the product Rhinallergy Kids which is product labeled by Boiron. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0220-9316-04 60 tablet in 1 blister pack . 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 Rhinallergy Kids?

Temporarily relieves one or more of these symptoms of hay fever or other upper respiratory allergies, itchy, watery eyes, sneezing, runny nose, itchy throat and nose

Which are Rhinallergy Kids UNII Codes?

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

Which are Rhinallergy Kids 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:

* Please review the disclaimer below.

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".