NDC 74220-003-07 - 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
- 74220-003
- Requested NDC
- 74220-003-07
- Package NDCs from labels
- 74220-003-01, 74220-003-03, 74220-003-04, 74220-003-05, 74220-003-06, 74220-003-07, 74220-003-17, 74220-003-02, 74220-003-08, 74220-003-09, 74220-003-10, 74220-003-11
- Manufacturer
- Super Dope Laboratories LLC
- Effective date
- 2020-06-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hand Sanitizer - Super Dope Laboratories LLC | Super Dope Laboratories LLC | 2020-06-25 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74220-003-01 | Hand Sanitizer | 60 mL in 1 BOTTLE | GEL | 60 | 6 | |
| 74220-003-02 | Hand Sanitizer | 100 mL in 1 BOTTLE | GEL | 100 | 6 | |
| 74220-003-03 | Hand Sanitizer | 120 mL in 1 BOTTLE | GEL | 120 | 6 | |
| 74220-003-04 | Hand Sanitizer | 500 mL in 1 BOTTLE | GEL | 500 | 6 | |
| 74220-003-05 | Hand Sanitizer | 750 mL in 1 BOTTLE | GEL | 750 | 6 | |
| 74220-003-06 | Hand Sanitizer | 1000 mL in 1 BOTTLE | GEL | 1000 | 6 | |
| 74220-003-07 | Hand Sanitizer | 2 mL in 1 PACKET | GEL | 2 | 6 | |
| 74220-003-08 | Hand Sanitizer | 3790 mL in 1 BOTTLE | GEL | 3790 | 6 | |
| 74220-003-09 | Hand Sanitizer | 1419528.75 mL in 1 DRUM | GEL | 1419528.75 | 6 | |
| 74220-003-10 | Hand Sanitizer | 355 mL in 1 BOTTLE | GEL | 355 | 6 | |
| 74220-003-11 | Hand Sanitizer | 237 mL in 1 BOTTLE | GEL | 237 | 6 | |
| 74220-003-17 | Hand Sanitizer | 100 in 1 BOX | GEL | 100 | 6 |
DailyMed Dashboard NDC Coverage#
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.