NDC 37205-607-05 - Leader Oral Pain Relief Anesthetic
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
- 37205-607
- Requested NDC
- 37205-607-05
- Package NDCs from labels
- 37205-607-05, 37205-607-06
- Manufacturer
- Cardinal Health | Lee Pharmaceuticals | Unipack
- Effective date
- 2012-08-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Benzocaine 20% - Cardinal Health | Lee Pharmaceuticals | Unipack | Cardinal Health | Lee Pharmaceuticals | Unipack | 2012-08-24 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 37205-607-06 | 2025-04-28 | C162847 | 48780-1 | 9d75b9d1-087f-f424-e053-dadaa90a57ce | Drug Facts |
| 37205-607-06 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-087f-f424-e053-dadaa90a57ce | Drug Facts |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Benzocaine | ACTIVE INGREDIENT | U3RSY48JW5 | LEADER ORAL PAIN RELIEF ANESTHETIC (BENZOCAINE 20%) GEL [CARDINAL HEALTH] | 11 | |
| Benzocaine | ACTIVE MOIETY | U3RSY48JW5 | LEADER ORAL PAIN RELIEF ANESTHETIC (BENZOCAINE 20%) GEL [CARDINAL HEALTH] | 11 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | LEADER ORAL PAIN RELIEF ANESTHETIC (BENZOCAINE 20%) GEL [CARDINAL HEALTH] | 11 | |
| SACCHARIN SODIUM DIHYDRATE | INACTIVE INGREDIENT | SB8ZUX40TY | LEADER ORAL PAIN RELIEF ANESTHETIC (BENZOCAINE 20%) GEL [CARDINAL HEALTH] | 11 | |
| Sorbic Acid | INACTIVE INGREDIENT | X045WJ989B | LEADER ORAL PAIN RELIEF ANESTHETIC (BENZOCAINE 20%) GEL [CARDINAL HEALTH] | 11 |
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.