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  4. NDC Product Code: 61010-4408 Antacid

NDC 61010-4408 Antacid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 61010-4408?
  5. 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:
61010-4408
Proprietary Name:
Antacid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Safetec Of America, Inc.
Labeler Code:
61010
Product Label ID:
fdc3a8b9-3edf-4339-9656-623973b32ea5
Start Marketing Date: [9]
12-30-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape:
ROUND (C48348)
Size(s):
16 MM
Imprint(s):
AP;052
Score:
1

Product Packages

NDC Code 61010-4408-0

Package Description: 2 TABLET in 1 POUCH

NDC Code 61010-4408-1

Package Description: 50 POUCH in 1 BOX / 2 TABLET in 1 POUCH (61010-4408-0)

NDC Code 61010-4408-2

Package Description: 100 POUCH in 1 BOX / 2 TABLET in 1 POUCH (61010-4408-0)

Product Details

What is NDC 61010-4408?

The NDC code 61010-4408 is assigned by the FDA to the product Antacid which is product labeled by Safetec Of America, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 61010-4408-0 2 tablet in 1 pouch , 61010-4408-1 50 pouch in 1 box / 2 tablet in 1 pouch (61010-4408-0), 61010-4408-2 100 pouch in 1 box / 2 tablet in 1 pouch (61010-4408-0). 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 Antacid?

This medication is used to treat symptoms caused by too much stomach acid such as heartburn, upset stomach, or indigestion. It is an antacid that works by lowering the amount of acid in the stomach. Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.

Which are Antacid UNII Codes?

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

Which are 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 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: 308915 - calcium carbonate 750 MG (Ca 300 MG) Chewable Tablet
  • RxCUI: 308915 - calcium carbonate 750 MG Chewable Tablet
  • RxCUI: 308915 - calcium carbonate 750 MG (calcium 300 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".