Hand wash
- Product NDC
- 51143-403
- 11-digit product format
- 511430403
- Labeler code
- 51143
- Product ID
- 51143-403_073f6c58-a5d8-4068-977f-7503b1adcd28
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Onpoint, Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-07-28
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 51143-403-64 | 51143040364 | 1893 mL in 1 BOTTLE, PLASTIC (51143-403-64) | 1893 ml | 2014-07-28 | 0000-00-00 | No | No | Current |
| 51143-403-96 | 51143040396 | 221 mL in 1 BOTTLE, PUMP (51143-403-96) | 221 ml | 2014-07-28 | 0000-00-00 | No | No | Current |