NDC 63868-303 Qc Quality Choice Pink Bismuth 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:
63868-303
Proprietary Name:
Qc Quality Choice Pink Bismuth Stomach Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chain Drug Manufacturing Assn
Labeler Code:
63868
Start Marketing Date: [9]
03-20-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)

Product Packages

NDC Code 63868-303-08

Package Description: 236 mL in 1 BOTTLE, PLASTIC

NDC Code 63868-303-12

Package Description: 354 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 63868-303?

The NDC code 63868-303 is assigned by the FDA to the product Qc Quality Choice Pink Bismuth Stomach Relief which is product labeled by Chain Drug Manufacturing Assn. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 63868-303-08 236 ml in 1 bottle, plastic , 63868-303-12 354 ml in 1 bottle, plastic . 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 Qc Quality Choice Pink Bismuth Stomach Relief?

•shake well before use•for accurate dosing, use dose cup•adults and children 12 years and over:1 dose (2 tbsp or 30 ml) every ½ to 1 hour as needed•do not exceed 8 doses (16 tbsp or 240 ml) in 24 hours•use until diarrhea stops but not more than 2 days•children under 12 years: ask a doctor•drink plenty of clear fluids to help prevent dehydration caused by diarrhea

Which are Qc Quality Choice Pink Bismuth Stomach Relief UNII Codes?

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

Which are Qc Quality Choice Pink Bismuth 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 Qc Quality Choice Pink Bismuth 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 indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 308762 - bismuth subsalicylate 525 MG in 30 mL Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 17.5 MG/ML Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 1.75 % Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 262 MG per 15 ML Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 524 MG per 30 ML Oral Suspension

* 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".