Anticavity
- Product NDC
- 49348-603
- 11-digit product format
- 493480603
- Labeler code
- 49348
- Product ID
- 49348-603_9584c012-e3f9-4021-9182-91b8eb526bd0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- McKesson
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2001-08-17
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49348-603-15 | ML - Milliliter | 49348-603 | 9afb1d91-270d-4373-ab6a-7fe1c3b83f8d | 1 | 2012-07-24 |