Label: D.S CRYSTAL TOOTH- calcium carbonate, sodium chloride paste, dentifrice

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated February 23, 2021

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENTS

    Calcium Carbonate 24.0%
    Sodium Chloride 3.0%

  • INACTIVE INGREDIENTS

    Sorbitol, Water, Glycerin, Erythritol, Silica, PEG-32, Sodium Lauryl Sulfate, Cellulose Gum, Sorbitan oleate, Menthol, Methylparaben, Mentha Piperita (Peppermint) Oil, Fragrance

  • PURPOSE

    Anti cavity

  • WARNINGS

    Adults and children 2 years of age and older: apply a 1-inch strip of product onto a toothbrush. Brush teeth thoroughly for 3 minutes three times a day (morning, afternoon, evening) or as recommended by a dentist. Do not swallow.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Uses

    ■ Helps fight and protect against cavities for healthier teeth.
    ■ Refresh your day with a strong mint flavor, which leaves your mouth feeling fresh and clean.

  • Directions

    ■ Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or three times a day, or as directed by a dentist or physician
    ■ Children 2 to 6 years: Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)
    ■ Children under 2 years: Consult a dentist

  • QUESTIONS

    ■ +82-31-837-8857

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    D.S CRYSTAL TOOTH 
    calcium carbonate, sodium chloride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81569-010
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Calcium Carbonate (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION28.8 g  in 120 g
    Sodium Chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) Sodium Chloride3.6 g  in 120 g
    Inactive Ingredients
    Ingredient NameStrength
    Sorbitol (UNII: 506T60A25R)  
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81569-010-021 in 1 CARTON02/01/2021
    1NDC:81569-010-01120 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/01/2021
    Labeler - Taeyang Crystal (688959504)
    Registrant - Taeyang Crystal (688959504)
    Establishment
    NameAddressID/FEIBusiness Operations
    EQMAXON Corp.557821534manufacture(81569-010)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!