FLAVON WHITE MINT TOOTH
- Product NDC
- 73660-003
- 11-digit product format
- 736600003
- Labeler code
- 73660
- Product ID
- 73660-003_c61ece91-4e52-4254-9f15-d46aaa7fa071
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium Carbonate, Allantoin
- Dosage form
- POWDER, DENTIFRICE
- Route
- ORAL
- Labeler
- BS and Co. Ltd
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-07-01
- Marketing end
- 0000-00-00
- Substance
- CALCIUM CARBONATE; ALLANTOIN
- Active strength
- 45 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 73660-003-01 | FLAVON WHITE MINT TOOTH | 50 g in 1 BOTTLE | POWDER, DENTIFRICE | 50 | | 1 |
| 73660-003-02 | FLAVON WHITE MINT TOOTH | 1 in 1 CARTON | POWDER, DENTIFRICE | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73660-003 | FLAVON WHITE MINT TOOTH (CALCIUM CARBONATE, ALLANTOIN) POWDER, DENTIFRICE [BS AND CO. LTD] | 1 | Legacy NDC, 2 package rows | 20200725_c57f91dd-19f2-404e-a4d7-dd47a0c505fd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73660-003-01 | 73660000301 | 50 g in 1 BOTTLE | 50 g | | | | | Historical |
| 73660-003-02 | 73660000302 | 1 BOTTLE in 1 CARTON (73660-003-02) > 50 g in 1 BOTTLE (73660-003-01) | 1 bottle | 2020-07-01 | 0000-00-00 | No | No | Current |