Durisan
- Product NDC
- 71120-612
- 11-digit product format
- 711200612
- Labeler code
- 71120
- Product ID
- 71120-612_fcccd426-1523-466f-9e3a-63a5a5f9ef2c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Sanit Technologies LLC
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-01-01
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 3 mg/250mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71120-612-02 | 71120061202 | 50 mL in 1 PACKAGE (71120-612-02) | 50 ml | 2016-01-01 | 0000-00-00 | No | No | Current |
| 71120-612-03 | 71120061203 | 250 mL in 1 PACKAGE (71120-612-03) | 250 ml | 2016-01-01 | 0000-00-00 | No | No | Current |
| 71120-612-04 | 71120061204 | 550 mL in 1 PACKAGE (71120-612-04) | 550 ml | 2016-01-01 | 0000-00-00 | No | No | Current |
| 71120-612-05 | 71120061205 | 1000 mL in 1 PACKAGE (71120-612-05) | 1000 ml | 2016-01-01 | 0000-00-00 | No | No | Current |
| 71120-612-06 | 71120061206 | 118 mL in 1 PACKAGE (71120-612-06) | 118 ml | 2016-01-01 | 0000-00-00 | No | No | Current |
| 71120-612-07 | 71120061207 | 236.58 mL in 1 PACKAGE (71120-612-07) | 236.58 ml | 2016-01-01 | 0000-00-00 | No | No | Current |
| 71120-612-08 | 71120061208 | 300 mL in 1 PACKAGE (71120-612-08) | 300 ml | 2016-01-01 | 0000-00-00 | No | No | Current |