NDC 0135-1326 Tums Naturals

NDC Product Code 0135-1326

NDC 0135-1326-01

Package Description: 56 TABLET, CHEWABLE in 1 BOTTLE

NDC 0135-1326-02

Package Description: 10 TABLET, CHEWABLE in 1 BOTTLE

NDC 0135-1326-03

Package Description: 190 TABLET, CHEWABLE in 1 BOTTLE

NDC 0135-1326-05

Package Description: 2 TABLET, CHEWABLE in 1 POUCH

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

NDC Product Information

Tums Naturals with NDC 0135-1326 is product labeled by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates multiple concept unique identifiers (RXCUI) are associated with this product:


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.

  • CALCIUM STEARATE (UNII: 776XM7047L)
  • DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
  • ACACIA (UNII: 5C5403N26O)

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: 10-15-2020 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: 12-31-2022 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 - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Tums Naturals 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 1000 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

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. Chew or crush tablets completely before swallowing. •do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Other Information

  • •each tablet contains: elemental calcium 400 mg •do not store above 25°C (77°F)

Inactive Ingredients (Black Cherry & Watermelon)

Calcium stearate, carmine, dextrose, flavors, gum arabic

Inactive Ingredients (Coconut Pineapple)

Calcium stearate, dextrose, flavor, gum arabic

* Please review the disclaimer below.