Hand Sanitizer
- Product NDC
- 51143-370
- 11-digit product format
- 511430370
- Labeler code
- 51143
- Product ID
- 51143-370_3a3da68b-f963-4ea9-b88d-17969047774d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Onpoint, Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-09-28
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 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 |
|---|
| 51143-370-16 | 51143037016 | 59 mL in 1 BOTTLE, PLASTIC (51143-370-16) | 59 ml | 2014-09-28 | 0000-00-00 | No | No | Current |
| 51143-370-34 | 51143037034 | 236 mL in 1 BOTTLE, PUMP (51143-370-34) | 236 ml | 2014-09-28 | 0000-00-00 | No | No | Current |