NDC 73097-010 Pepto-bismol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 73097-010?
What are the uses for Pepto-bismol?
Which are Pepto-bismol UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Pepto-bismol 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)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- POVIDONE (UNII: FZ989GH94E)
- D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Pepto-bismol?
- RxCUI: 308760 - bismuth subsalicylate 262 MG Oral Tablet
- RxCUI: 702384 - Pepto-Bismol 262 MG Oral Tablet
- RxCUI: 702384 - bismuth subsalicylate 262 MG Oral Tablet [Pepto-bismol]
- RxCUI: 702384 - Pepto-bismol 262 MG Oral 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".