Instant Hand Sanitizer
- Product NDC
- 75589-101
- 11-digit product format
- 755890101
- Labeler code
- 75589
- Product ID
- 75589-101_a64c5e41-c5c5-0c86-e053-2995a90a781c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- 75% alcohol
- Dosage form
- GEL
- Route
- EXTRACORPOREAL
- Labeler
- Zhejiang Yangxiang Technology Co., Ltd
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 75 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 75589-101-01 | 75589010101 | 30 mL in 1 BOTTLE (75589-101-01) | 30 ml | 2020-05-01 | 0000-00-00 | No | No | Current |
| 75589-101-02 | 75589010102 | 60 mL in 1 BOTTLE (75589-101-02) | 60 ml | 2020-03-30 | 0000-00-00 | No | No | Current |
| 75589-101-03 | 75589010103 | 60 mL in 1 BOTTLE (75589-101-03) | 60 ml | 2020-05-01 | 0000-00-00 | Yes | No | Current |
| 75589-101-15 | 75589010115 | 300 mL in 1 BOTTLE (75589-101-15) | 300 ml | 2020-05-01 | 0000-00-00 | No | No | Current |
| 75589-101-25 | 75589010125 | 500 mL in 1 BOTTLE (75589-101-25) | 500 ml | 2020-05-01 | 0000-00-00 | No | No | Current |