Foaming Hand Sanitizer
- Product NDC
- 73782-207
- Requested package NDC
- 73782-207-10
- 11-digit product format
- 737820207
- Labeler code
- 73782
- Product ID
- 73782-207_d6e3fd07-5af7-fc17-e053-2a95a90a91c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol-Free Foaming Hand Sanitizer
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Chemco Corporation
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-16
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 mg/mL
- 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 |
|---|
| 73782-207-10 | 73782020710 | 1000 mL in 1 BAG (73782-207-10) | 1000 ml | 2020-03-16 | 0000-00-00 | No | No | Current |