Oral-B
- Product NDC
- 0041-1421
- 11-digit product format
- 000411421
- Labeler code
- 0041
- Product ID
- 0041-1421_64705480-a0f6-4765-8dc4-7ae64816d3a4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- LIQUID
- Route
- DENTAL
- Labeler
- Oral-B Laboratories
- Application
- part355
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2005-10-15
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 500 ug/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 0041-1421-16 | Oral-B Anticavity | 500 mL in 1 BOTTLE, PLASTIC | LIQUID | 500 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0041-1421 | ORAL-B (SODIUM FLUORIDE) LIQUID [ORAL-B LABORATORIES] | 1 | Legacy NDC, 1 package rows | 20100420_d8336ad5-d1fb-4290-9433-d852405d1409.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 0041-1421-16 | 00041142116 | 500 mL in 1 BOTTLE, PLASTIC | 500 ml | Historical |