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  4. NDC Product Code: 63868-178 Multi Symptom Antacid Berry Flavor

NDC 63868-178 Multi Symptom Antacid Berry Flavor

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63868-178?
  5. Multi Symptom Antacid Berry Flavor 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:
63868-178
Proprietary Name:
Multi Symptom Antacid Berry Flavor
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Quality Choice (chain Drug Marketing Association)
Labeler Code:
63868
Product Label ID:
4a044668-ec7f-4379-ab01-73d394586c30
Start Marketing Date: [9]
04-17-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - PINKISH)
Shape:
ROUND (C48348)
Size(s):
16 MM
Imprint(s):
RP107
Score:
1
Flavor(s):
BERRY (C73365)

Code Structure Chart

Product Details

What is NDC 63868-178?

The NDC code 63868-178 is assigned by the FDA to the product Multi Symptom Antacid Berry Flavor which is product labeled by Quality Choice (chain Drug Marketing Association). The product's dosage form is . The product is distributed in a single package with assigned NDC code 63868-178-10 100 tablet, chewable 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 Multi Symptom Antacid Berry Flavor?

▪chew 2-4 tablets completely as symptoms occur or as directed by a doctor.

Which are Multi Symptom Antacid Berry Flavor UNII Codes?

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

Which are Multi Symptom Antacid Berry Flavor 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 Multi Symptom Antacid Berry Flavor?

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: 476553 - calcium carbonate 675 MG / magnesium hydroxide 135 MG / simethicone 60 MG Chewable Tablet
  • RxCUI: 476553 - calcium carbonate 675 MG / milk of magnesia 135 MG / simethicone 60 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]


Magnesium Hydroxide


Magnesium hydroxide is used to treat occasional constipation in children and adults on a short-term basis. Magnesium hydroxide is in a class of medications called saline laxatives. It works by causing water to be retained with the stool. This increases the number of bowel movements and softens the stool so it is easier to pass.
[Learn More]


Simethicone


Simethicone is used to treat the symptoms of gas such as uncomfortable or painful pressure, fullness, and bloating. 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".