Hand Sanitizer Alcohol 80%
- Product NDC
- 78232-001
- 11-digit product format
- 782320001
- Labeler code
- 78232
- Product ID
- 78232-001_c78ea356-5e1d-b65a-e053-2a95a90ad0cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Clarity Labs LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-07-31
- Marketing end
- 2023-06-23
- Substance
- ALCOHOL
- Active strength
- 80 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 78232-001-01 | 78232000101 | 60 mL in 1 BOTTLE (78232-001-01) | 60 ml | 2020-07-31 | 0000-00-00 | No | No | Current |
| 78232-001-02 | 78232000102 | 240 mL in 1 BOTTLE (78232-001-02) | 240 ml | 2020-07-31 | 0000-00-00 | No | No | Current |
| 78232-001-03 | 78232000103 | 500 mL in 1 BOTTLE (78232-001-03) | 500 ml | 2020-07-31 | 0000-00-00 | No | No | Current |
| 78232-001-04 | 78232000104 | 3700 mL in 1 BOTTLE (78232-001-04) | 3700 ml | 2020-07-31 | 0000-00-00 | No | No | Current |