Label: DR.NOAH MARUTOOTHPASTE- precipitated calcium carbonate paste

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated October 29, 2021

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  • ACTIVE INGREDIENT

    precipitated calcium carbonate

  • INACTIVE INGREDIENT

    d-sorbitol solution, water, concentrated glycerin, scutellaria bak, alensls root extract, xanthan gurn, sodium cocoyl glutamate, sodium
    cocoyl isethionate, 1-mentho~ steviol, glycoside, xylitol, mentha pulagium, oil, peppermint oil, spearmint oil, sodium chloride, silicon dioxide

  • PURPOSE

    ■ Keeps teeth white and strong

    ■ Keep the oral cavity clean

    ■ Prevents tooth decay and bad breath caused by fluoride

    ■ Removing plaque, preventing gingivitis and periodontitis

    ■ Periodontal Disease Prevention

    ■ Gum Disease Prevention

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • WARNING

    For oral use only
    When using this product

    ■ This toothpaste has a 1,000 ppm fluoride content

    ■ Do not use other than brushing teeth and be careful not to swallow

    Keep out of reach of children

    ■ if swallowed, seek medical help or contact the poison control center immediately

  • USES

    for oral use only

  • INDICATION & USAGE SECTION

    Brush thoroughly ofter each meal or at least twice a day, as directed by yourdoctorordendst
    Do not swallow.

    Do not use if seal is broken or missing.

    store in a cool, dry place.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DR.NOAH MARUTOOTHPASTE 
    precipitated calcium carbonate paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82359-0002
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION0.22 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SORBITOL (UNII: 506T60A25R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82359-0002-1120 g in 1 TUBE; Type 0: Not a Combination Product10/29/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/29/2021
    Labeler - DR.Noah (695333875)
    Registrant - DR.Noah (695333875)
    Establishment
    NameAddressID/FEIBusiness Operations
    DONG IL PHARMS CO., LTD.557810721manufacture(82359-0002)
    Establishment
    NameAddressID/FEIBusiness Operations
    DR.Noah695333875label(82359-0002)
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