YOUZHI Hand Sanitizer
- Product NDC
- 53023-001
- 11-digit product format
- 530230001
- Labeler code
- 53023
- Product ID
- 53023-001_a34c2a92-a33b-3e2a-e053-2995a90af772
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- YOUZHI Hand Sanitizer
- Dosage form
- GEL
- Route
- EXTRACORPOREAL
- Labeler
- Hubei Mulan Tongda Technology Co., Ltd
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-04-15
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 375 mL/500mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53023-001-01 | YOUZHI Hand Sanitizer | 500 mL in 1 BOTTLE | GEL | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53023-001 | YOUZHI HAND SANITIZER GEL [HUBEI MULAN TONGDA TECHNOLOGY CO., LTD] | 1 | Legacy NDC, 1 package rows | 20200415_a34c2a92-a33a-3e2a-e053-2995a90af772.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 |
|---|
| 53023-001-01 | 53023000101 | 500 mL in 1 BOTTLE (53023-001-01) | 500 ml | 2020-04-15 | 0000-00-00 | No | No | Current |