NDC 74010-3010 - Hand Sanitizer USA
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
- 74010-3010
- Package NDCs from labels
- 74010-3010-1, 74010-3010-2, 74010-3010-4, 74010-3010-3, 74010-3010-5, 74010-3010-6
- Manufacturer
- Global Universal SRL LLC dba Minhas Micro Distillery
- Effective date
- 2020-04-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hand Sanitizer USA - Global Universal SRL LLC dba Minhas Micro Distillery | Global Universal SRL LLC dba Minhas Micro Distillery | 2020-04-07 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74010-3010-1 | Hand Sanitizer | 50 mL in 1 BOTTLE, PLASTIC | LIQUID | 50 | 2 | |
| 74010-3010-2 | Hand Sanitizer | 200 mL in 1 BOTTLE, PLASTIC | LIQUID | 200 | 2 | |
| 74010-3010-3 | Hand Sanitizer | 375 mL in 1 BOTTLE, PLASTIC | LIQUID | 375 | 2 | |
| 74010-3010-4 | Hand Sanitizer | 1000 mL in 1 BOTTLE, PLASTIC | LIQUID | 1000 | 2 | |
| 74010-3010-5 | Hand Sanitizer | 1140 mL in 1 BOTTLE, PLASTIC | LIQUID | 1140 | 2 | |
| 74010-3010-6 | Hand Sanitizer | 750 mL in 1 BOTTLE, PLASTIC | LIQUID | 750 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 74010-3010 | HAND SANITIZER USA LIQUID HAND SANITIZER (ALCOHOL) LIQUID [GLOBAL UNIVERSAL SRL LLC DBA MINHAS MICRO DISTILLERY] | 2 | 6 package rows | 20200408_a1c461af-5f23-085c-e053-2995a90a12da.zip |
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.