ANTIBACTERIAL HANDWASH
- Product NDC
- 73789-0440
- 11-digit product format
- 737890440
- Labeler code
- 73789
- Product ID
- 73789-0440_a2034c5c-0b2c-2980-e053-2995a90a75cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Hobi Kozmetik Imalat Sanayi Ve Ticaret Anonim Sirketi
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-02-05
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.