DiaSinc
- Product NDC
- 59088-596
- 11-digit product format
- 590880596
- Labeler code
- 59088
- Product ID
- 59088-596_2385c911-b836-5c8c-e063-6394a90ad257
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- PureTek Corporation
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-03-24
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1.3 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F5UM2KM3W7 | BENZALKONIUM CHLORIDE | 8001-54-5 | BENZALKONIUM CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59088-596-16 | 59088059616 | 237 mL in 1 BOTTLE, SPRAY (59088-596-16) | 237 ml | 2023-03-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| DiaSinc | PureTek Corporation | 2024-10-02 | HUMAN OTC DRUG LABEL | 2 |