NDC 70000-0459 Leader Ultra Strength Peppermint Flavor

NDC Product Code 70000-0459

NDC 70000-0459-1

Package Description: 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Product Information

Leader Ultra Strength Peppermint Flavor with NDC 70000-0459 is a product labeled by Cardinal Health. The generic name of Leader Ultra Strength Peppermint Flavor is . The product's dosage form is and is administered via form.

Labeler Name: Cardinal Health

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.

  • DEXTROSE (UNII: IY9XDZ35W2)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Labeler Information

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

Labeler Name: Cardinal Health
Labeler Code: 70000
Start Marketing Date: 12-18-2018 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: 12-31-2020 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: E 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’.

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Information for Patients



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Calcium Carbonate

Calcium Carbonate is pronounced as (kal' see um) (kar' bon ate)
Why is calcium carbonate medication prescribed?
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, nervo...
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Leader Ultra Strength Peppermint Flavor Product Label Images

Leader Ultra Strength Peppermint Flavor 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 presently taking 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 at room temperature. Keep container tightly closed.

Inactive Ingredients

Dextrose, flavors, magnesium stearate, maltodextrin, starch, sucralose.

Questions?

1-866-467-2748 Safety sealed: Do not use if printed seal under cap is torn or missing

* Please review the disclaimer below.