Durisan
- Product NDC
- 71120-114
- 11-digit product format
- 711200114
- Labeler code
- 71120
- Product ID
- 71120-114_2c197f2a-e1a3-4857-84b0-436b50c27892
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Sanit Technologies LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-10-08
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71120-114-01 | Durisan | 300 mL in 1 PACKAGE | LIQUID | 300 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71120-114 | DURISAN (BENZALKONIUM CHLORIDE) LIQUID [SANIT TECHNOLOGIES LLC] | 1 | Legacy NDC, 1 package rows | 20201010_07d48c66-4f1e-40c5-9cc8-bbb37de05537.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71120-114-01 | 71120011401 | 300 mL in 1 PACKAGE (71120-114-01) | 300 ml | 2020-10-08 | 0000-00-00 | No | No | Current |