Antibacterial
- Product NDC
- 69790-640
- Requested package NDC
- 69790-640-24
- 11-digit product format
- 697900640
- Labeler code
- 69790
- Product ID
- 69790-640_ded53cbe-0d8a-3832-e053-2a95a90ab54e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- Uline
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-09-12
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- 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 |
|---|
| 69790-640-24 | 69790064024 | 1000 mL in 1 BAG (69790-640-24) | 1000 ml | 2017-09-12 | 0000-00-00 | No | No | Current |