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  4. NDC Product Code: 54473-203 Calmicid Ac Acid Reducer

NDC 54473-203 Calmicid Ac Acid Reducer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54473-203?
  5. Calmicid Ac Acid Reducer Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.
NDC Product Code:
54473-203
Proprietary Name:
Calmicid Ac Acid Reducer
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Melaleuca, Inc.
Labeler Code:
54473
Product Label ID:
9aed4009-307c-44ef-8dce-394a8d4c6597
Start Marketing Date: [9]
01-20-2011
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape:
ROUND (C48348)
Size(s):
8 MM
Imprint(s):
L194
Score:
1

Code Structure Chart

Product Details

What is NDC 54473-203?

The NDC code 54473-203 is assigned by the FDA to the product Calmicid Ac Acid Reducer which is product labeled by Melaleuca, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54473-203-50 1 bottle in 1 box / 50 tablet, film coated in 1 bottle (54473-203-01). 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 Calmicid Ac Acid Reducer?

Userelieves heartburn associated with acid indigestion and sour stomachprevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food and beverages

Which are Calmicid Ac Acid Reducer UNII Codes?

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

Which are Calmicid Ac Acid Reducer 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 Calmicid Ac Acid Reducer?

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

Famotidine


Prescription famotidine is used to treat ulcers (sores on the lining of the stomach or small intestine); gastroesophageal reflux disease (GERD, a condition in which backward flow of acid from the stomach causes heartburn and injury of the esophagus [tube that connects the mouth and stomach]); and conditions where the stomach produces too much acid, such as Zollinger-Ellison syndrome (tumors in the pancreas or small intestine that cause increased production of stomach acid). Over-the-counter famotidine is used to prevent and treat heartburn due to acid indigestion and sour stomach caused by eating or drinking certain foods or drinks. Famotidine is in a class of medications called H2 blockers. It works by decreasing the amount of acid made in the stomach.
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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".