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  4. NDC Product Code: 63736-044 Bonine Kids

NDC 63736-044 Bonine Kids

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63736-044?
  5. Bonine Kids Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63736-044
Proprietary Name:
Bonine Kids
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Insight Pharmaceuticals
Labeler Code:
63736
Product Label ID:
9220360a-67d3-4a14-ba21-304a06697cd4
Start Marketing Date: [9]
06-08-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
ROUND (C48348)
Size(s):
14 MM
Imprint(s):
BONINE
Score:
2
Flavor(s):
BERRY (C73365)

Code Structure Chart

Product Details

What is NDC 63736-044?

The NDC code 63736-044 is assigned by the FDA to the product Bonine Kids which is product labeled by Insight Pharmaceuticals. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 63736-044-08 8 tablet, chewable in 1 box , 63736-044-12 12 tablet, chewable in 1 box . 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 Bonine Kids?

Children 6 years of age and older: chew 1 tablet thoroughly every 6 to 8 hoursdo not exceed 3 tablets in 24 hours or as directed by a doctordosage should be taken up to one hour before travel starts or at onset of symptoms

Which are Bonine Kids UNII Codes?

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

Which are Bonine 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:

What is the NDC to RxNorm Crosswalk for Bonine Kids?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".