Zest Aqua Antibacterial Hand
- Product NDC
- 20890-1794
- 11-digit product format
- 208901794
- Labeler code
- 20890
- Product ID
- 20890-1794_d53e2d37-0f8a-6983-e053-2995a90af4cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- Abaco Partners LLC DBA Surefil
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-12-15
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 13 mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 20890-1794-1 | 20890179401 | 221 mL in 1 BOTTLE, PUMP (20890-1794-1) | 221 ml | 2020-07-15 | 0000-00-00 | No | No | Current |