D.S Crystal Tooth
- Product NDC
- 81569-010
- 11-digit product format
- 815690010
- Labeler code
- 81569
- Product ID
- 81569-010_a8472661-767f-4803-9d4b-9cc83b9bf5d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium Carbonate, Sodium Chloride
- Dosage form
- PASTE, DENTIFRICE
- Route
- ORAL
- Labeler
- Taeyang Crystal
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-02-01
- Marketing end
- 0000-00-00
- Substance
- CALCIUM CARBONATE; SODIUM CHLORIDE
- Active strength
- 29 g/120g; g/120g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| 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#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81569-010 | D.S CRYSTAL TOOTH (CALCIUM CARBONATE, SODIUM CHLORIDE) PASTE, DENTIFRICE [TAEYANG CRYSTAL] | 1 | Legacy NDC, 2 package rows | 20210224_3998b486-1f08-4115-bf7d-017167425a61.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81569-010-01 | 81569001001 | 120 g in 1 TUBE | 120 g | | | | | Historical |
| 81569-010-02 | 81569001002 | 1 TUBE in 1 CARTON (81569-010-02) > 120 g in 1 TUBE (81569-010-01) | 1 tube | 2021-02-01 | 0000-00-00 | No | No | Current |