HAND SANITIZER
- Product NDC
- 41366-073
- Requested package NDC
- 41366-073-01
- 11-digit product format
- 413660073
- Labeler code
- 41366
- Product ID
- 41366-073_eb225f45-90b6-eb3e-e053-2a95a90aaca4
- 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
- 2022-10-12
- 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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41366-073-01 | 41366007301 | 59 mL in 1 BOTTLE (41366-073-01) | 59 ml | 2022-10-12 | 0000-00-00 | No | No | Current |