Hand Sanitizer
- Product NDC
- 0519-8802
- 11-digit product format
- 005198802
- Labeler code
- 0519
- Product ID
- 0519-8802_8361e31b-986f-47f9-a5a2-843e6f0b3858
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Steris Corporation
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-09-08
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 578 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0519-8802-13 | 00519880213 | 444 mL in 1 BOTTLE, PLASTIC (0519-8802-13) | 444 ml | 2014-09-08 | 0000-00-00 | No | No | Current |
| 0519-8802-41 | 00519880241 | 1000 mL in 1 BOTTLE, PLASTIC (0519-8802-41) | 1000 ml | 2014-09-08 | 0000-00-00 | No | No | Current |