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

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81569-010
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Calcium Carbonate (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	28.8 g in 120 g
Sodium Chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	Sodium Chloride	3.6 g in 120 g

Ingredient Name	Strength
Inactive Ingredients
Sorbitol (UNII: 506T60A25R)
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:81569-010-02	1 in 1 CARTON	02/01/2021
1	NDC:81569-010-01	120 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		02/01/2021

Labeler - Taeyang Crystal (688959504)

Registrant - Taeyang Crystal (688959504)

Name	Address	ID/FEI	Business Operations
Establishment
EQMAXON Corp.		557821534	manufacture(81569-010)