D.S CRYSTAL TOOTH- calcium carbonate, sodium chloride paste, dentifrice 
Taeyang Crystal

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.

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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

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)

Revised: 2/2021
Document Id: a8472661-767f-4803-9d4b-9cc83b9bf5d6
Set id: 3998b486-1f08-4115-bf7d-017167425a61
Version: 1
Effective Time: 20210223
 
Taeyang Crystal