NDC 37205-720 Leader Stomach Relief Original Strength

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:
37205-720
Proprietary Name:
Leader Stomach Relief Original Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cardinal Health
Labeler Code:
37205
Start Marketing Date: [9]
08-20-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
ROUND (C48348)
Size(s):
17 MM
Imprint(s):
L469
Score:
1

Product Packages

NDC Code 37205-720-65

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

Price per Unit: $0.07799 per EA

Product Details

What is NDC 37205-720?

The NDC code 37205-720 is assigned by the FDA to the product Leader Stomach Relief Original Strength which is product labeled by Cardinal Health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 37205-720-65 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 Leader Stomach Relief Original Strength?

▪chew or dissolve tablets in mouth▪drink plenty of clear fluids to help prevent dehydration caused by diarrhea▪adults and children 12 years and older: 2 tablets every ½ to 1 hour, or 4 tablets every hour as needed▪do not exceed 16 tablets in 24 hours▪use until diarrhea stops but not more than 2 days▪children under 12 years: ask a doctor

Which are Leader Stomach Relief Original Strength UNII Codes?

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

Which are Leader Stomach Relief Original Strength 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 Leader Stomach Relief Original Strength?

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:

* Please review the disclaimer below.

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]


* 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".