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  4. NDC Product Code: 75981-012 Goodsense Antacid Fruit Chews

NDC 75981-012 Goodsense Antacid Fruit Chews

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 75981-012?
  5. Goodsense Antacid Fruit Chews Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
75981-012
Proprietary Name:
Goodsense Antacid Fruit Chews
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Geiss, Destin & Dunn
Labeler Code:
75981
Product Label ID:
c5ffaaee-0f78-4a13-e053-2995a90ad6ba
Start Marketing Date: [9]
06-30-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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):
ORANGE (C73406 - ORANGE, STRAWBERRY, & LEMON)

Code Structure Chart

Product Details

What is NDC 75981-012?

The NDC code 75981-012 is assigned by the FDA to the product Goodsense Antacid Fruit Chews which is product labeled by Geiss, Destin & Dunn. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75981-012-32 32 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 Goodsense Antacid Fruit Chews?

Uses Relieves HeartburnSour stomachAcid indigestionUpset stomach due to these symptoms

Which are Goodsense Antacid Fruit Chews UNII Codes?

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

Which are Goodsense Antacid Fruit 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 Goodsense Antacid Fruit 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.

Patient Education

Calcium Carbonate


Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]


* 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".