Antibacterial
- Product NDC
- 50157-601
- Requested package NDC
- 50157-601-44
- 11-digit product format
- 501570601
- Labeler code
- 50157
- Product ID
- 50157-601_ed76c513-2329-40ec-e053-2995a90a020d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Brands International Corporation
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-09-06
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/1000mL
- 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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50157-601-44 | 50157060144 | 443.6 mL in 1 BOTTLE, PUMP (50157-601-44) | 443.6 ml | 2022-09-06 | 0000-00-00 | No | No | Current |