75% Alcohol Hand Sanitizer Gel
- Product NDC
- 10884-8001
- 11-digit product format
- 108848001
- Labeler code
- 10884
- Product ID
- 10884-8001_a334df49-1c50-4b34-a650-df7c338eb2fa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bright Future Pharmaceutical Laboratories Limited
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-26
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 1 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 10884-8001-2 | 10884800102 | 60 mL in 1 BOTTLE (10884-8001-2) | 60 ml | 2020-05-26 | 0000-00-00 | No | No | Current |
| 10884-8001-3 | 10884800103 | 500 mL in 1 BOTTLE (10884-8001-3) | 500 ml | 2020-06-01 | 0000-00-00 | No | No | Current |