NDC 21130-469 Upset Stomach Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21130 - Safeway
- 21130-469 - Upset Stomach Relief
Product Characteristics
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?
What are the uses for Upset Stomach Relief?
Which are Upset Stomach Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1)
- BISMUTH CATION (UNII: ZS9CD1I8YE) (Active Moiety)
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:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Upset Stomach Relief?
- RxCUI: 308761 - bismuth subsalicylate 262 MG Chewable Tablet
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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.
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[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".