NDC 0135-0181 Tums Ultra

Calcium Carbonate Tablet, Chewable Oral - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
0135-0181
Proprietary Name:
Tums Ultra
Non-Proprietary Name: [1]
Calcium Carbonate
Substance Name: [2]
Calcium Carbonate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Haleon Us Holdings Llc
    Labeler Code:
    0135
    FDA Application Number: [6]
    M001
    Marketing Category: [8]
    OTC MONOGRAPH DRUG -
    Start Marketing Date: [9]
    02-12-2010
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

    Color(s):
    PINK (C48328 - ORANGE, YELLOW, GREEN)
    ORANGE (C48331 - RED-ORANGE, CREAM TO OFF-WHITE, LIGHT YELLOW)
    PINK (C48328 - MAUVE, BLUISH)
    Shape:
    ROUND (C48348)
    Size(s):
    19 MM
    Imprint(s):
    TUMS
    Score:
    1
    Flavor(s):
    CHERRY (C73375 - ASSORTED FRUIT, ORANGE, LEMON, LIME)
    TROPICAL FRUIT PUNCH (C73419 - ASSORTED TROPICAL FRUIT, MANDARIN ORANGE, ORANGE-PINEAPPLE, STRAWBERRY-BANANA)
    BERRY (C73365 - ASSORTED BERRY, STRAWBERRY, RASPBERRY, MIXED BERRY)

    Product Packages

    NDC Code 0135-0181-01

    Package Description: 3 PACKAGE in 1 CARTON / 12 TABLET, CHEWABLE in 1 PACKAGE

    Price per Unit: $0.05254 per EA

    NDC Code 0135-0181-02

    Package Description: 72 TABLET, CHEWABLE in 1 BOTTLE

    Price per Unit: $0.05254 per EA

    NDC Code 0135-0181-03

    Package Description: 12 TABLET, CHEWABLE in 1 PACKAGE

    Price per Unit: $0.05585 per EA

    NDC Code 0135-0181-05

    Package Description: 265 TABLET, CHEWABLE in 1 BOTTLE

    Price per Unit: $0.05254 per EA

    NDC Code 0135-0181-06

    Package Description: 86 TABLET, CHEWABLE in 1 BOTTLE

    NDC Code 0135-0181-07

    Package Description: 1 PACKAGE in 1 CARTON / 12 TABLET, CHEWABLE in 1 PACKAGE

    NDC Code 0135-0181-14

    Package Description: 160 TABLET, CHEWABLE in 1 BOTTLE

    Price per Unit: $0.05254 per EA

    Product Details

    What is NDC 0135-0181?

    The NDC code 0135-0181 is assigned by the FDA to the product Tums Ultra which is a human over the counter drug product labeled by Haleon Us Holdings Llc. The generic name of Tums Ultra is calcium carbonate. The product's dosage form is tablet, chewable and is administered via oral form. The product is distributed in 7 packages with assigned NDC codes 0135-0181-01 3 package in 1 carton / 12 tablet, chewable in 1 package, 0135-0181-02 72 tablet, chewable in 1 bottle , 0135-0181-03 12 tablet, chewable in 1 package , 0135-0181-05 265 tablet, chewable in 1 bottle , 0135-0181-06 86 tablet, chewable in 1 bottle , 0135-0181-07 1 package in 1 carton / 12 tablet, chewable in 1 package, 0135-0181-14 160 tablet, chewable in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Tums Ultra?

    This medication is used to treat symptoms caused by too much stomach acid such as heartburn, upset stomach, or indigestion. It is an antacid that works by lowering the amount of acid in the stomach. Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.

    What are Tums Ultra Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • CALCIUM CARBONATE 1000 mg/1 - Carbonic acid calcium salt (CaCO3). An odorless, tasteless powder or crystal that occurs in nature. It is used therapeutically as a phosphate buffer in hemodialysis patients and as a calcium supplement.

    Which are Tums Ultra UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Tums Ultra 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. The UNII codes for the inactive ingredients in this product are:

    What is the NDC to RxNorm Crosswalk for Tums Ultra?

    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:

    * Please review the disclaimer below.

    Patient Education

    Calcium Carbonate


    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, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
    [Learn More]


    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] 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.

    [12] 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".