Foaming Antibacterial Hand
- Product NDC
- 61307-640
- 11-digit product format
- 613070640
- Labeler code
- 61307
- Product ID
- 61307-640_d6e7f16e-b103-8a47-e053-2a95a90a771b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lavish Antibacterial
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- US Chemical Corporation
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-10-28
- 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 |
|---|
| 61307-640-10 | 61307064010 | 1000 mL in 1 BAG (61307-640-10) | 1000 ml | 2018-10-28 | 0000-00-00 | No | No | Current |