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  4. NDC Product Code: 49035-169 Ultra Strength Antacid Assorted Fruit

NDC 49035-169 Ultra Strength Antacid Assorted Fruit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 49035-169?
  5. Ultra Strength Antacid Assorted Fruit Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
49035-169
Proprietary Name:
Ultra Strength Antacid Assorted Fruit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wal-mart Stores,inc.,
Labeler Code:
49035
Product Label ID:
a1021774-4d7a-4e44-807e-95103aa82c40
Start Marketing Date: [9]
11-25-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
GREEN (C48329)
YELLOW (C48330)
ORANGE (C48331)
Shape:
ROUND (C48348)
Size(s):
19 MM
Imprint(s):
RP103
Score:
1
Flavor(s):
FRUIT (C73389 - ASSORTED FRUIT)

Product Packages

NDC Code 49035-169-16

Package Description: 160 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

Product Details

What is NDC 49035-169?

The NDC code 49035-169 is assigned by the FDA to the product Ultra Strength Antacid Assorted Fruit which is product labeled by Wal-mart Stores,inc.,. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49035-169-16 160 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 Ultra Strength Antacid Assorted Fruit?

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 Ultra Strength Antacid Assorted Fruit UNII Codes?

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

Which are Ultra Strength Antacid Assorted Fruit 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 Ultra Strength Antacid Assorted Fruit?

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: 308892 - calcium carbonate 1000 MG (Ca 400 MG) Chewable Tablet
  • RxCUI: 308892 - calcium carbonate 1000 MG Chewable Tablet
  • RxCUI: 308892 - calcium carbonate 1000 MG (calcium 400 MG) Chewable Tablet

* 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".