NDC 24673-712 - GFS BioProtect Aloe Vera 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
- 24673-712
- Package NDCs from labels
- 24673-712-21, 24673-712-22
- Manufacturer
- RWM TECHNOLOGIES
- Effective date
- 2011-09-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| GFS BioProtect Aloe Vera Hand Sanitizer - RWM TECHNOLOGIES | RWM TECHNOLOGIES | 2011-09-13 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 24673-712-21 | GFS BioProtect Aloe Vera Hand Sanitizer | 1006000 g in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK | GEL | 1006000 | 8 | |
| 24673-712-22 | GFS BioProtect Aloe Vera Hand Sanitizer | 2012000 g in 1 DRUM | GEL | 2012000 | 8 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.