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  4. NDC Product Code: 73659-015 Rapidcare Flavored Antacid

NDC 73659-015 Rapidcare Flavored Antacid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 73659-015?
  5. Rapidcare Flavored Antacid 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 data was inactivated by the FDA.
NDC Product Code:
73659-015
Proprietary Name:
Rapidcare Flavored Antacid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rapid Care, Inc
Labeler Code:
73659
Product Label ID:
dcf5ce51-35b2-3f29-e053-2a95a90ababb
Start Marketing Date: [9]
04-18-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Shape:
ROUND (C48348)
Size(s):
16 MM
Flavor(s):
CHERRY (C73375)

Product Packages

NDC Code 73659-015-01

Package Description: 50 POUCH in 1 BOX / 2 TABLET, CHEWABLE in 1 POUCH

NDC Code 73659-015-02

Package Description: 125 POUCH in 1 BOX / 2 TABLET, CHEWABLE in 1 POUCH

Product Details

What is NDC 73659-015?

The NDC code 73659-015 is assigned by the FDA to the product Rapidcare Flavored Antacid which is product labeled by Rapid Care, Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 73659-015-01 50 pouch in 1 box / 2 tablet, chewable in 1 pouch, 73659-015-02 125 pouch in 1 box / 2 tablet, chewable in 1 pouch. 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 Rapidcare Flavored Antacid?

This product is used as Antacid. Relieves  heartburn  sour stomach  acid indigestion  upset stomach associated with these symptoms

Which are Rapidcare Flavored Antacid UNII Codes?

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

Which are Rapidcare Flavored Antacid 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 Rapidcare Flavored Antacid?

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: 313884 - calcium carbonate 420 MG (Ca 168 MG) Chewable Tablet
  • RxCUI: 313884 - calcium carbonate 420 MG Chewable Tablet
  • RxCUI: 313884 - calcium carbonate 420 MG (calcium 168 MG) Chewable Tablet

* Please review the disclaimer below.

Patient Education

Calcium Carbonate


Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[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".