NDC 74737-2011-3 - 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
- 74737-2011
- Requested NDC
- 74737-2011-3
- Package NDCs from labels
- 74737-2011-1, 74737-2011-8, 74737-2011-3, 74737-2011-0, 74737-2011-4, 74737-2011-6, 74737-2011-5, 74737-2011-7
- Manufacturer
- Zhejiang Yuantiao Cosmetics Co., Ltd. | A03 Lab of BTS
- Effective date
- 2020-05-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| HAND SANITIZER - Zhejiang Yuantiao Cosmetics Co., Ltd. | A03 Lab of BTS | Zhejiang Yuantiao Cosmetics Co., Ltd. | A03 Lab of BTS | 2020-05-28 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74737-2011-0 | HAND SANITIZER | 48 in 1 CARTON | GEL | 48 | 3 | |
| 74737-2011-1 | HAND SANITIZER | 55 mL in 1 BOTTLE | GEL | 55 | 3 | |
| 74737-2011-3 | HAND SANITIZER | 250 mL in 1 BOTTLE | GEL | 250 | 3 | |
| 74737-2011-4 | HAND SANITIZER | 300 mL in 1 BOTTLE | GEL | 300 | 3 | |
| 74737-2011-5 | HAND SANITIZER | 3785 mL in 1 BOTTLE | GEL | 3785 | 3 | |
| 74737-2011-6 | HAND SANITIZER | 48 in 1 CARTON | GEL | 48 | 3 | |
| 74737-2011-7 | HAND SANITIZER | 4 in 1 CARTON | GEL | 4 | 3 | |
| 74737-2011-8 | HAND SANITIZER | 240 in 1 CARTON | GEL | 240 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 74737-2011 | HAND SANITIZER (ALCOHOL) GEL [ZHEJIANG YUANTIAO COSMETICS CO., LTD.] | 3 | Legacy NDC, 8 package rows | 20200526_a2f53d77-187a-4fcb-e053-2a95a90a2735.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.