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

NDC Product Code 11673-903

NDC 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.

NDC Product Information

Up And Up Ultra Strength Antacid Assorted Fruit with NDC 11673-903 is a product labeled by Target Corporation. The generic name of Up And Up Ultra Strength Antacid Assorted Fruit is . The product's dosage form is and is administered via form.

Labeler Name: Target Corporation

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • ADIPIC ACID (UNII: 76A0JE0FKJ)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • DEXTROSE (UNII: IY9XDZ35W2)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • D&C RED NO. 27 (UNII: 2LRS185U6K)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • SUCRALOSE (UNII: 96K6UQ3ZD4)
  • FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
  • D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Target Corporation
Labeler Code: 11673
Start Marketing Date: 10-22-2015 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: 12-31-2019 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: I 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Information for Patients



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* Please review the disclaimer below.

Up And Up Ultra Strength Antacid Assorted Fruit Product Label Images

Up And Up Ultra Strength Antacid Assorted Fruit Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient (Per Tablet)

Calcium Carbonate USP 1000mg

Purpose

Antacid

Uses

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

Warnings

  • 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.

Directions

  • 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.

Questions?

1-866-467-2748

* Please review the disclaimer below.