NDC 0135-0070 Tums

NDC Product Code 0135-0070

NDC 0135-0070-03

Package Description: 3 PACKAGE in 1 CELLO PACK > 12 TABLET in 1 PACKAGE

NDC 0135-0070-27

Package Description: 150 TABLET in 1 BOTTLE

NDC 0135-0070-48

Package Description: 12 TABLET in 1 PACKAGE

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

NDC Product Information

Tums with NDC 0135-0070 is a product labeled by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The generic name of Tums is . The product's dosage form is and is administered via form.

Labeler Name: Glaxosmithkline Consumer Healthcare Holdings (us) Llc

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)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)
  • SUCROSE (UNII: C151H8M554)
  • TALC (UNII: 7SEV7J4R1U)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)
  • SUCROSE (UNII: C151H8M554)
  • TALC (UNII: 7SEV7J4R1U)

Product Labeler Information

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

Labeler Name: Glaxosmithkline Consumer Healthcare Holdings (us) Llc
Labeler Code: 0135
Start Marketing Date: 03-10-2010 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: 12-31-2018 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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[Read More]
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...
[Read More]

* Please review the disclaimer below.

Tums 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 500 mg

Purpose

Antacid

Uses

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

Ask A Doctor Or Pharmacist Before Use If You Are

Taking a prescription drug. Antacids may interact with certain prescription drugs.

When Using This Product

  • •do not take more than 15 tablets in 24 hours •if pregnant do not take more than 10 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 2-4 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

Other Information

  • •each tablet contains: elemental calcium 200mg •store below 30oC (86oF)

Inactive Ingredients (Assorted Fruit)

Adipic acid, corn starch, FD&C blue #1 lake, FD&C red #40 lake, FD&C yellow #5 (tartrazine) lake, FD&C yellow #6 lake, flavors, mineral oil, sodium polyphosphate, sucrose, talc

Inactive Ingredient (Peppermint)

Corn starch, flavor, mineral oil, sodium polyphosphate, sucrose, talc

Questions?

1-800-897-7535weekdaysSafety sealed- Do not use if printed inner seal beneath cap is missing or broken.Gluten-Freewww.tums.comGlaxoSmithKlineMoon Twp, PA 15108

* Please review the disclaimer below.