E3 Foaming Hand Sanitizer Problend
- Product NDC
- 76250-110
- 11-digit product format
- 762500110
- Labeler code
- 76250
- Product ID
- 76250-110_f679c9ef-689d-4953-a6d2-f85e21787fc8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Seatex Ltd
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-05-08
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 g/1000mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#