NDC 47682-302-99 - Antiseptic
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
- 47682-302
- Requested NDC
- 47682-302-99
- Package NDCs from labels
- 47682-302-99, 47682-302-73
- Manufacturer
- Unifirst First Aid Corporation | Safetec of America, Inc.
- Effective date
- 2020-02-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Green Guard Antiseptic Wipes | Unifirst First Aid Corporation | Safetec of America, Inc. | 2020-02-17 | HUMAN OTC DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| benzalkonium chloride | ACTIVE INGREDIENT | F5UM2KM3W7 | ANTISEPTIC (BENZALKONIUM CHLORIDE) LIQUID [UNIFIRST FIRST AID CORPORATION] | 1 | |
| benzalkonium | ACTIVE MOIETY | 7N6JUD5X6Y | ANTISEPTIC (BENZALKONIUM CHLORIDE) LIQUID [UNIFIRST FIRST AID CORPORATION] | 1 | |
| alcohol | INACTIVE INGREDIENT | 3K9958V90M | ANTISEPTIC (BENZALKONIUM CHLORIDE) LIQUID [UNIFIRST FIRST AID CORPORATION] | 1 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | ANTISEPTIC (BENZALKONIUM CHLORIDE) LIQUID [UNIFIRST FIRST AID CORPORATION] | 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.