Dental Pro
- Product NDC
- 41525-6001
- 11-digit product format
- 415256001
- Labeler code
- 41525
- Product ID
- 41525-6001_d4edc948-7977-4452-9808-7dad09319d54
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- MOUTHWASH
- Route
- DENTAL
- Labeler
- PBS Co., Ltd.
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-09-11
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 mg/100mL
- 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 |
|---|
| 41525-6001-1 | Dental Pro | 250 mL in 1 BOTTLE | MOUTHWASH | 250 | | 1 |
| 41525-6001-2 | Dental Pro | 600 mL in 1 BOTTLE | MOUTHWASH | 600 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41525-6001 | DENTAL PRO (SODIUM FLUORIDE) MOUTHWASH [PBS CO., LTD.] | 1 | Legacy NDC, 2 package rows | 20140911_a500f313-7085-4f29-bd2d-cf14bbfdaec4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 41525-6001-1 | 41525600101 | 250 mL in 1 BOTTLE | 250 ml | Historical |
| 41525-6001-2 | 41525600102 | 600 mL in 1 BOTTLE | 600 ml | Historical |