NDC 64778-0396-2 - Denti-Care Denti-Freeze Topical Anesthetic Mint
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
- 64778-0396
- Requested NDC
- 64778-0396-2
- Package NDCs from labels
- 64778-0396-1, 64778-0396-2, 64778-0396-3
- 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 |
|---|---|---|---|
| 10039-M Mint Topical DentiCare Pro-Freeze Topical Anesthetic Gel | 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 MINT (BENZOCAINE, TETRACAINE HYDROCHLORIDE) GEL [AR MEDICOM INC] | 1 | |
| tetracaine hydrochloride | ACTIVE INGREDIENT | 5NF5D4OPCI | DENTI-CARE DENTI-FREEZE TOPICAL ANESTHETIC MINT (BENZOCAINE, TETRACAINE HYDROCHLORIDE) GEL [AR MEDICOM INC] | 1 | |
| benzocaine | ACTIVE MOIETY | U3RSY48JW5 | DENTI-CARE DENTI-FREEZE TOPICAL ANESTHETIC MINT (BENZOCAINE, TETRACAINE HYDROCHLORIDE) GEL [AR MEDICOM INC] | 1 | |
| tetracaine | ACTIVE MOIETY | 0619F35CGV | DENTI-CARE DENTI-FREEZE TOPICAL ANESTHETIC MINT (BENZOCAINE, TETRACAINE HYDROCHLORIDE) GEL [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.