NDC 21749-689 - PURELL SF607 Foam Hand Rub Benzalkonium Chloride Solution Non Alcohol
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
- 21749-689
- Package NDCs from labels
- 21749-689-89
- Manufacturer
- GOJO Industries, Inc.
- Effective date
- 2021-07-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PURELL SF607 Foam Hand Rub Benzalkonium Chloride Solution Non Alcohol | GOJO Industries, Inc. | 2021-07-09 | HUMAN OTC DRUG LABEL |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| CVS Pain Relieving First Aid Antiseptic | LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE | CVS Pharmacy | 454b1773-eda8-5610-e054-00144ff88e88 | 2017-01-04 | Warnings | F5UM2KM3W7 |
| CVS Pharmacy Sensitive Medicated Cream | BENZOCAINE, BENZALKONIUM CHLORIDE | CVS Pharmacy | 454c3458-7e40-0e5e-e054-00144ff8d46c | 2017-01-04 | Warnings | F5UM2KM3W7 |
| Sit Clean | BENZALKONIUM CHLORIDE | Sit Clean | ef2b12f8-89b3-47c4-88bd-8712a84cfc45 | 2016-08-18 | Warnings | F5UM2KM3W7 |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.