NDC 67239-0221-01 - Safco Sensicaine Ultra Topical Anesthetic Gel
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
- 67239-0221
- Requested NDC
- 67239-0221-01
- Package NDCs from labels
- 67239-0221-1, 67239-0221-01
- Manufacturer
- Safco Dental Supply Co.
- Effective date
- 2025-01-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Safco Sensicaine Ultra Topical Anesthetic Gel - Safco Dental Supply Co. | Safco Dental Supply Co. | 2025-01-08 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67239-0221-1 | Safco Sensicaine Ultra Topical Anesthetic Gel | 30 g in 1 JAR | GEL | 30 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 67239-0221 | SAFCO SENSICAINE ULTRA TOPICAL ANESTHETIC GEL (BENZOCAINE) GEL [SAFCO DENTAL SUPPLY CO.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250110_923614c5-d1bf-b444-e053-2995a90aa5c6.zip |
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.