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  4. NDC Product Code: 55319-017 Antacid Fruit Flavor Chews

NDC 55319-017 Antacid Fruit Flavor Chews

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 55319-017?
  5. Antacid Fruit Flavor Chews 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:
55319-017
Proprietary Name:
Antacid Fruit Flavor Chews
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Family Dollar
Labeler Code:
55319
Product Label ID:
63b2ede2-17bf-cdf7-e053-2a91aa0a5cbf
Start Marketing Date: [9]
01-26-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331 - ORANGE, PINK, YELLOW)
Shape:
ROUND (C48348)
Size(s):
14 MM
Imprint(s):
FC
Score:
1
Flavor(s):
FRUIT (C73389 - LEMON, ORANGE, STRAWBERRY)

Product Packages

NDC Code 55319-017-36

Package Description: 36 LOZENGE in 1 BOTTLE

Product Details

What is NDC 55319-017?

The NDC code 55319-017 is assigned by the FDA to the product Antacid Fruit Flavor Chews which is product labeled by Family Dollar. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55319-017-36 36 lozenge 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 Antacid Fruit Flavor Chews?

Uses RelievesHeartburnSour stomachAcid indigestionUpset stomach due to these symptoms

Which are Antacid Fruit Flavor Chews UNII Codes?

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

Which are Antacid Fruit Flavor Chews 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 Antacid Fruit Flavor Chews?

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".