NDC 21130-469 Upset Stomach Relief

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
21130-469
Proprietary Name:
Upset Stomach Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Safeway
Labeler Code:
21130
Start Marketing Date: [9]
08-08-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
ROUND (C48348)
Size(s):
17 MM
Imprint(s):
GDC122
Score:
1

Product Packages

NDC Code 21130-469-65

Package Description: 5 BLISTER PACK in 1 CARTON / 6 TABLET, CHEWABLE in 1 BLISTER PACK

Product Details

What is NDC 21130-469?

The NDC code 21130-469 is assigned by the FDA to the product Upset Stomach Relief which is product labeled by Safeway. The product's dosage form is . The product is distributed in a single package with assigned NDC code 21130-469-65 5 blister pack in 1 carton / 6 tablet, chewable in 1 blister pack. 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 Upset Stomach Relief?

Chew or dissolve in mouthadults and children 12 years and over: 2 tablets every 1/2 to 1 hour as neededdo not take more than 8 doses (16 tablets) in 24 hourschildren under 12 years: ask a doctordrink plenty of clear fluids to help prevent dehydration caused by diarrhea.Other information: each tablet contains:sodium less than 1 mgsalicylate 102 mgcalcium 140 mgvery low sodiumavoid excessive heat (over 104˚F or 40˚C)TAMPER EVIDENT: Do not use if individual compartments are torn or missing.

Which are Upset Stomach Relief UNII Codes?

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

Which are Upset Stomach Relief 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 Upset Stomach Relief?

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 code indicates a single concept unique identifier (RXCUI) is associated with this product:

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Patient Education

Bismuth Subsalicylate


Bismuth subsalicylate is used to treat diarrhea, heartburn, and upset stomach in adults and children 12 years of age and older. Bismuth subsalicylate is in a class of medications called antidiarrheal agents. It works by decreasing the flow of fluids and electrolytes into the bowel, reduces inflammation within the intestine, and may kill the organisms that can cause diarrhea.
[Learn More]


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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".