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  4. NDC Product Code: 52642-227 Assorted Fruit

NDC 52642-227 Assorted Fruit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52642-227?
  5. Assorted Fruit 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:
52642-227
Proprietary Name:
Assorted Fruit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bestco Inc
Labeler Code:
52642
Product Label ID:
2bd093ea-ad8b-5b27-e054-00144ff8d46c
Start Marketing Date: [9]
08-31-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
YELLOW (C48330)
PINK (C48328)
Shape:
ROUND (C48348)
Size(s):
70 MM
Imprint(s):
AS
Flavor(s):
LEMON (C73396)
ORANGE (C73406)
STRAWBERRY (C73417)

Code Structure Chart

Product Details

What is NDC 52642-227?

The NDC code 52642-227 is assigned by the FDA to the product Assorted Fruit which is product labeled by Bestco Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52642-227-36 36 tablet, chewable in 1 bottle . 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 Assorted Fruit?

Uses for the relief of: acid indigestionheartburnsour stomachupset stomach associated with these symptoms

Which are Assorted Fruit UNII Codes?

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

Which are Assorted Fruit 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 Assorted Fruit?

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:
  • RxCUI: 308915 - calcium carbonate 750 MG (Ca 300 MG) Chewable Tablet
  • RxCUI: 308915 - calcium carbonate 750 MG Chewable Tablet
  • RxCUI: 308915 - calcium carbonate 750 MG (calcium 300 MG) Chewable Tablet

* 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".