NDC 65321-025-04 - Foam Hand Sanitizer
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
- 65321-025
- Requested NDC
- 65321-025-04
- Package NDCs from labels
- 65321-025-03, 65321-025-01, 65321-025-04, 65321-025-02
- Manufacturer
- Rubbermaid Commercial Products LLC | NWL Netherlands Production B.V.
- Effective date
- 2014-02-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| TC ® ENRICHEDFOAM™ Alcohol Plus Hand Sanitizer | Rubbermaid Commercial Products LLC | NWL Netherlands Production B.V. | 2014-02-20 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 65321-025-01 | 2023-10-27 | TC ® ENRICHEDFOAM™ Alcohol Plus Hand Sanitizer |
| 65321-025-02 | 2023-10-27 | TC ® ENRICHEDFOAM™ Alcohol Plus Hand Sanitizer |
| 65321-025-01 | 2019-11-27 | TC ® ENRICHEDFOAM™ Alcohol Plus Hand Sanitizer |
| 65321-025-02 | 2019-11-27 | TC ® ENRICHEDFOAM™ Alcohol Plus Hand Sanitizer |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Alcohol | ACTIVE INGREDIENT | 3K9958V90M | FOAM HAND SANITIZER (ALCOHOL) LIQUID [RUBBERMAID COMMERCIAL PRODUCTS LLC] | 2 | |
| Alcohol | ACTIVE MOIETY | 3K9958V90M | FOAM HAND SANITIZER (ALCOHOL) LIQUID [RUBBERMAID COMMERCIAL PRODUCTS LLC] | 2 | |
| Lactic Acid | INACTIVE INGREDIENT | 33X04XA5AT | FOAM HAND SANITIZER (ALCOHOL) LIQUID [RUBBERMAID COMMERCIAL PRODUCTS LLC] | 2 | |
| Sodium Lactate | INACTIVE INGREDIENT | TU7HW0W0QT | FOAM HAND SANITIZER (ALCOHOL) LIQUID [RUBBERMAID COMMERCIAL PRODUCTS LLC] | 2 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | FOAM HAND SANITIZER (ALCOHOL) LIQUID [RUBBERMAID COMMERCIAL PRODUCTS LLC] | 2 |
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.