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  4. NDC Product Code: 67060-304 Cherry Antacid

NDC 67060-304 Cherry Antacid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67060-304?
  5. Cherry 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:
67060-304
Proprietary Name:
Cherry Antacid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Advanced First Aid, Inc.
Labeler Code:
67060
Product Label ID:
6dbd58f4-4329-4d6a-895a-3a1b20e4db60
Start Marketing Date: [9]
04-07-2015
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328 - ROSE PINK)
Shape:
ROUND (C48348)
Size(s):
12 MM
Imprint(s):
FR8
Score:
1
Flavor(s):
CHERRY (C73375)

Product Packages

NDC Code 67060-304-67

Package Description: 250 PACKET in 1 CARTON / 2 TABLET, CHEWABLE in 1 PACKET

NDC Code 67060-304-68

Package Description: 100 PACKET in 1 CARTON / 2 TABLET, CHEWABLE in 1 PACKET

Product Details

What is NDC 67060-304?

The NDC code 67060-304 is assigned by the FDA to the product Cherry Antacid which is product labeled by Advanced First Aid, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 67060-304-67 250 packet in 1 carton / 2 tablet, chewable in 1 packet, 67060-304-68 100 packet in 1 carton / 2 tablet, chewable in 1 packet. 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 Cherry Antacid?

Uses:for the relief of:•heartburn • sour stomach • acid indigestion

Which are Cherry Antacid UNII Codes?

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

Which are Cherry 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 Cherry 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".