NDC 11673-903 Up And Up Ultra Strength Antacid Assorted Fruit

Product Information

What is NDC 11673-903?

The NDC code 11673-903 is assigned by the FDA to the product Up And Up Ultra Strength Antacid Assorted Fruit which is product labeled by Target Corporation. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 11673-903-17 160 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, RxNorm crosswalk and the complete product label.

NDC Product Code11673-903
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Up And Up Ultra Strength Antacid Assorted Fruit
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Target Corporation
Labeler Code11673
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date 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.
Exclude Flag 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".
NDC Code Structure

What are the uses for Up And Up Ultra Strength Antacid Assorted Fruit?

Product Characteristics

Color(s)RED (C48326)
GREEN (C48329)
YELLOW (C48330)
ORANGE (C48331)
ShapeROUND (C48348)
Size(s)19 MM
Flavor(s)FRUIT (C73389 - ASSORTED FRUIT)

Product Packages

NDC Code 11673-903-17

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

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Up And Up Ultra Strength Antacid Assorted Fruit Active Ingredients UNII Codes

NDC to RxNorm Crosswalk

What is RxNorm? 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

Up And Up 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.

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Patient Education


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Up And Up Ultra Strength Antacid Assorted Fruit Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents

Active Ingredient (Per Tablet)

Calcium Carbonate USP 1000mg





  • •heartburn
  • •acid indigestion
  • •sour stomach
  • •upset stomach associated with these symptoms


Ask a doctor or pharmacist before use if you are presentlytaking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

  •  do not take more than 7 tablets in 24 hours
  •  if pregnant do not take more than 5 tablets in 24 hours
  •  do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor.


  •  adults and children 12 years of age and over: chew 2-3 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

Other Information

  •  each tablet contains: elemental calcium 400mg
  •  store below 30°C (86°F).

Inactive Ingredients

adipic acid, blue 1, dextrose, flavors, magnesium stearate, maltodextrin, red 27, starch, sucralose, yellow 6 lake, yellow 10 lake.



Package/Label Principal Display Panel

NDC 11673-903-17

Compare to Tums Ultra®*

ultra strength

antacid 1000

calcium carbonate

relief of heartburn, acid indigestion ,sour stomach and upset stomach associated with these symptoms




naturally and artificially flavored

245 05 0457 R00


Distributed by

Target Corporation

Minneapolis, MN 55403

©2016 Target Brands, Inc.

*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark Tums®.


Safety sealed: Do not use if printed seal under cap is torn or missing

100% satisfaction guaranteed or your money back.

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