NDC 49035-102 Equate Extra Strength Antacid Wintergreen

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
49035-102
Proprietary Name:
Equate Extra Strength Antacid Wintergreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wal-mart Stores,inc.,
Labeler Code:
49035
Start Marketing Date: [9]
10-07-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
GREEN (C48329)
ORANGE (C48331)
RED (C48326)
Shape:
ROUND (C48348)
Size(s):
16 MM
Imprint(s):
RP102
Score:
1
Flavor(s):
FRUIT (C73389 - ASSORTED)

Product Packages

NDC Code 49035-102-02

Package Description: 1 BOTTLE in 1 BOTTLE / 30 mL in 1 BOTTLE (49035-102-01)

NDC Code 49035-102-14

Package Description: 96 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

NDC Code 49035-102-24

Package Description: 96 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

NDC Code 49035-102-28

Package Description: 200 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

NDC Code 49035-102-54

Package Description: 96 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

Product Details

What is NDC 49035-102?

The NDC code 49035-102 is assigned by the FDA to the product Equate Extra Strength Antacid Wintergreen which is product labeled by Wal-mart Stores,inc.,. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 49035-102-02 1 bottle in 1 bottle / 30 ml in 1 bottle (49035-102-01), 49035-102-14 96 tablet, chewable in 1 bottle, plastic , 49035-102-24 96 tablet, chewable in 1 bottle, plastic , 49035-102-28 200 tablet, chewable in 1 bottle, plastic , 49035-102-54 96 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 Equate Extra Strength Antacid Wintergreen?

 •adults and children 12 years of ageand over: chew 2-4 tablets as symptoms occur, or as directed by a doctor•do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Which are Equate Extra Strength Antacid Wintergreen UNII Codes?

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

Which are Equate Extra Strength Antacid Wintergreen 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 Equate Extra Strength Antacid Wintergreen?

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".