NDC 64778-0499-2 - Denti-Care Denti-Freeze Topical Anesthetic Strawberry
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 64778-0499
- Requested NDC
- 64778-0499-2
- Package NDCs from labels
- 64778-0499-1, 64778-0499-2, 64778-0499-3
- Manufacturer
- AMD Medicom Inc.
- Effective date
- 2020-12-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 10049-ST Strawberry Ointment Denti-Care Denti-Freeze Topical Anesthetic | AMD Medicom Inc. | 2020-12-09 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| benzocaine | ACTIVE INGREDIENT | U3RSY48JW5 | DENTI-CARE DENTI-FREEZE TOPICAL ANESTHETIC STRAWBERRY (BENZOCAINE) OINTMENT [AR MEDICOM INC] | 1 | |
| benzocaine | ACTIVE MOIETY | U3RSY48JW5 | DENTI-CARE DENTI-FREEZE TOPICAL ANESTHETIC STRAWBERRY (BENZOCAINE) OINTMENT [AR MEDICOM INC] | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.