Hand Sanitizer
- Product NDC
- 41366-051
- 11-digit product format
- 413660051
- Labeler code
- 41366
- Product ID
- 41366-051_dcebf021-9d6a-bfae-e053-2a95a90a0510
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hand Sanitizer
- Dosage form
- GEL
- Route
- EXTRACORPOREAL
- Labeler
- Zhejiang Meimi Technology Co., Ltd.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-04-18
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41366-051-01 | Hand Sanitizer | 59 mL in 1 BOTTLE | GEL | 59 | | 2 |
| 41366-051-02 | Hand Sanitizer | 59 mL in 1 BOTTLE | GEL | 59 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41366-051 | HAND SANITIZER GEL [ZHEJIANG MEIMI TECHNOLOGY CO., LTD.] | 2 | Legacy NDC, 2 package rows | 20240121_dcebf021-9d6b-bfae-e053-2a95a90a0510.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41366-051-01 | 41366005101 | 59 mL in 1 BOTTLE (41366-051-01) | 59 ml | 2022-04-18 | 0000-00-00 | No | No | Current |
| 41366-051-02 | 41366005102 | 59 mL in 1 BOTTLE (41366-051-02) | 59 ml | 2022-04-18 | 0000-00-00 | No | No | Current |