Whitening Foaming-Toothpaste
- Product NDC
- 75902-2001
- 11-digit product format
- 759022001
- Labeler code
- 75902
- Product ID
- 75902-2001_96986790-e17a-494c-8008-e60e0702d743
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Dio Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-10-04
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE; ALLANTOIN
- Active strength
- 0 mL/mL; mL/mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75902-2001-1 | Whitening Foaming-Toothpaste | 50 mL in 1 BOTTLE, PUMP | GEL, DENTIFRICE | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75902-2001 | WHITENING FOAMING-TOOTHPASTE (SODIUM FLUORIDE) GEL, DENTIFRICE [DIO CORPORATION] | 1 | Legacy NDC, 1 package rows | 20111005_6f019744-35a4-487d-9c42-ccb6095d9b5d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 75902-2001-1 | 75902200101 | 50 mL in 1 BOTTLE, PUMP | 50 ml | Historical |