Foaming Hand Wash
- Product NDC
- 64542-213
- 11-digit product format
- 645420213
- Labeler code
- 64542
- Product ID
- 64542-213_d6e827e7-5f39-fd0a-e053-2a95a90a2a35
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antibacterial Hand Wash
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- State Industrial Products
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-02-14
- 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 |
|---|
| 64542-213-09 | 64542021309 | 3785 mL in 1 BOTTLE (64542-213-09) | 3785 ml | 2019-02-14 | 0000-00-00 | No | No | Current |
| 64542-213-41 | 64542021341 | 1000 mL in 1 BAG (64542-213-41) | 1000 ml | 2019-02-14 | 0000-00-00 | No | No | Current |