Indications and 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.
D.S Crystal Tooth
- Manufacturer
- Taeyang Crystal | EQMAXON Corp.
- Effective date
- 2021-02-23
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:38:27
Label at a glance#
ProductD.S Crystal Tooth
Active ingredientCalcium Carbonate, Sodium Chloride
Label structure9 sections
Dosage and administration
■ 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
Label contents#
Full prescribing information#
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
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| CALCIUM CATION Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20230427 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81569-010-02 | 2023-01-30 | C162847 | 48780-1 | f386c649-bd68-0266-e053-dadaa90a7c1a | 3998b486-1f08-4115-bf7d-017167425a61 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81569-010-01 | D.S Crystal Tooth | 120 g in 1 TUBE | PASTE, DENTIFRICE | 120 | 1 | |
| 81569-010-02 | D.S Crystal Tooth | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- D.S Crystal Tooth
- Calcium Carbonate, Sodium Chloride
- Calcium Carbonate
- CALCIUM CATION
- Sodium Chloride
- CHLORIDE ION
- Sorbitol
- Water
- Glycerin
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 81569-010 | 81569-010-01, 81569-010-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Calcium Carbonate | H0G9379FGK | ACTIM |
| Sodium Chloride | 451W47IQ8X | ACTIB |
| Sorbitol | 506T60A25R | IACT |
| Water | 059QF0KO0R | IACT |
| Glycerin | PDC6A3C0OX | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| a8472661-767f-4803-9d4b-9cc83b9bf5d6 | 3998b486-1f08-4115-bf7d-017167425a61 | 2021-02-23 | Warnings | a8472661-767f-4803-9d4b-9cc83b9bf5d6 3998b486-1f08-4115-bf7d-017167425a61 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.