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  4. NDC Product Code: 67091-226 Antacid Ultra Strength Assorted Berries

NDC 67091-226 Antacid Ultra Strength Assorted Berries

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67091-226?
  5. Antacid Ultra Strength Assorted Berries 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:
67091-226
Proprietary Name:
Antacid Ultra Strength Assorted Berries
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Winco Foods, Llc
Labeler Code:
67091
Product Label ID:
5a0b9985-a38e-4991-a653-5ded733e9e7e
Start Marketing Date: [9]
12-12-2014
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
BLUE (C48333)
PINK (C48328 - BLUE-PINK)
Shape:
ROUND (C48348)
Size(s):
17 MM
Imprint(s):
G171
Score:
1
Flavor(s):
BERRY (C73365 - STRAWBERRY, RASPBERRY, WILDBERRY)

Code Structure Chart

Product Details

What is NDC 67091-226?

The NDC code 67091-226 is assigned by the FDA to the product Antacid Ultra Strength Assorted Berries which is product labeled by Winco Foods, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67091-226-72 72 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 Antacid Ultra Strength Assorted Berries?

Chew 2-3 tablets as symptoms occur, or as directed by a doctor.Other informationdo not use if printed seal under cap is torn or missingstore at room temperature

Which are Antacid Ultra Strength Assorted Berries UNII Codes?

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

Which are Antacid Ultra Strength Assorted Berries 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 Ultra Strength Assorted Berries?

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: 308892 - calcium carbonate 1000 MG (Ca 400 MG) Chewable Tablet
  • RxCUI: 308892 - calcium carbonate 1000 MG Chewable Tablet
  • RxCUI: 308892 - calcium carbonate 1000 MG (calcium 400 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".