Personal CARE Foaming Hand Sanitizer
- Product NDC
- 20276-142
- 11-digit product format
- 202760142
- Labeler code
- 20276
- Product ID
- 20276-142_eaee8ac1-ca38-01ac-e053-2a95a90aaf47
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Delta Brands Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-31
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
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 |
|---|
| 20276-142-08 | 20276014208 | 236 mL in 1 BOTTLE, PUMP (20276-142-08) | 236 ml | 2020-08-31 | 0000-00-00 | No | No | Current |