Advanced Hand Sanitizer
- Product NDC
- 51143-439
- 11-digit product format
- 511430439
- Labeler code
- 51143
- Product ID
- 51143-439_816fc227-7341-4bfb-9ac8-a62aff4a5fd7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Onpoint, Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-09-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 700 mg/mL
- 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 |
|---|
| 51143-439-16 | 51143043916 | 59 mL in 1 BOTTLE, DISPENSING (51143-439-16) | 59 ml | 2014-09-30 | 0000-00-00 | No | No | Current |
| 51143-439-34 | 51143043934 | 236 mL in 1 BOTTLE, PUMP (51143-439-34) | 236 ml | 2014-09-30 | 0000-00-00 | No | No | Current |