Finefra Black Tooth
- Product NDC
- 69653-110
- 11-digit product format
- 696530110
- Labeler code
- 69653
- Product ID
- 69653-110_555dae8c-0e23-4b4a-9ce4-2c5417619a64
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SILICON DIOXIDE, ALCLOXA
- Dosage form
- PASTE, DENTIFRICE
- Route
- TOPICAL
- Labeler
- Jewoo Medical Co,.Ltd
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-12-01
- Marketing end
- 0000-00-00
- Substance
- SILICON DIOXIDE; ALCLOXA
- Active strength
- 20 g/135g; g/135g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 69653-110-01 | Finefra Black Tooth | 135 g in 1 TUBE | PASTE, DENTIFRICE | 135 | | 1 |
| 69653-110-02 | Finefra Black 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 |
|---|
| 69653-110 | FINEFRA BLACK TOOTH (SILICON DIOXIDE, ALCLOXA) PASTE, DENTIFRICE [JEWOO MEDICAL CO,.LTD] | 1 | Legacy NDC, 2 package rows | 20191226_117060c4-5298-4027-bfb9-7db1a347a8d7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69653-110-01 | 69653011001 | 135 g in 1 TUBE | 135 g | | | | | Historical |
| 69653-110-02 | 69653011002 | 1 TUBE in 1 CARTON (69653-110-02) > 135 g in 1 TUBE (69653-110-01) | 1 tube | 2019-12-01 | 0000-00-00 | No | No | Current |