Label: NUTRALOX- calcium carbonate tablet, chewable

  • NDC Code(s): 50332-0151-1, 50332-0151-3, 50332-0151-4, 50332-0151-7, view more
    50332-0151-8
  • Packager: HART Health
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 9, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient (in each tablet): Calcium Carbonate 420 mg

  • PURPOSE

    Purpose: Antacid

  • INDICATIONS & USAGE

    Uses: Temporarily relieves

    • heartburn
    • sour stomach
    • acid indigestion
    • upset stomach
  • WARNINGS

    Warnings:

  • ASK DOCTOR/PHARMACIST

    Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interfere with certain prescription drugs.

  • STOP USE

    Stop use and ask a doctor if symptoms last for more than 2 weeks

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. 1-800-222-1222

  • DOSAGE & ADMINISTRATION

    Directions:

    Do not take more than directed

    Adults and children 12 years of age and over:

    • thoroughly chew 2 tablets every 3 to 4 hours as symptoms occur
    • do not take more than 16 tablets in 24 hours unless directed by a doctor
    • do not use the maximum dose for more than 2 weeks

    Children under 12 years of age: ask a doctor

  • OTHER SAFETY INFORMATION

    Other information:

    • Calcium content per tablet: 168mg
    • phenylketonurics: each tablet may contain 1.5 mg phenylalanine
    • tablets enclosed in a sealed packet
    • do not use if packet is torn, cut or open
    • store at 59° to 86°F (15°-30°C)
    • avoid excessive heat and humidity
  • INACTIVE INGREDIENT

    Inactive ingredients

    aspartame, croscarmellose sodium, magnesium stearate, maltodextrin, mint flavor, sorbitol

    May contain mineral oil

  • PRINCIPAL DISPLAY PANEL

    Nutralox.jpg

  • INGREDIENTS AND APPEARANCE
    NUTRALOX 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50332-0151
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE420 mg
    Inactive Ingredients
    Ingredient NameStrength
    ASPARTAME (UNII: Z0H242BBR1)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize11mm
    FlavorImprint Code AZ;036
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50332-0151-320 in 1 BOX, UNIT-DOSE01/20/1987
    12 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:50332-0151-450 in 1 BOX, UNIT-DOSE01/20/1987
    22 in 1 PACKET; Type 0: Not a Combination Product
    3NDC:50332-0151-7125 in 1 BOX, UNIT-DOSE01/20/1987
    32 in 1 PACKET; Type 0: Not a Combination Product
    4NDC:50332-0151-8250 in 1 BOX, UNIT-DOSE01/20/1987
    42 in 1 PACKET; Type 0: Not a Combination Product
    5NDC:50332-0151-1500 in 1 BOX, UNIT-DOSE01/20/1987
    52 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01/20/1987
    Labeler - HART Health (069560969)
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