HYVEE
- Product NDC
- 42507-554
- 11-digit product format
- 425070554
- Labeler code
- 42507
- Product ID
- 42507-554_6ad57f6e-a256-4f25-9206-cf0822da1a50
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- HYVEE INC.
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-11-29
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 42507-554-17 | HYVEEANTICAVITY MINT | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42507-554 | HYVEE ANTICAVITY MINT (SODIUM FLUORIDE) LIQUID [HYVEE INC.] | 2 | Legacy NDC, 1 package rows | 20151130_8cca3d39-1df2-4e83-af2b-1f6599dfb27b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 42507-554-17 | 42507055417 | 473 mL in 1 BOTTLE, PLASTIC | 473 ml | Historical |