GenRx Hand Sanitizing
- Product NDC
- 59088-315
- 11-digit product format
- 590880315
- Labeler code
- 59088
- Product ID
- 59088-315_2385f398-8cf7-8437-e063-6394a90a78a4
- 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
- 2020-03-18
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1.3 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- GenRx Hand Sanitizing
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1.3 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1039012 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59088-315-16 | GenRx Hand Sanitizing | 237 mL in 1 BOTTLE, SPRAY | SPRAY | 237 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59088-315 | GENRX HAND SANITIZING (BENZALKONIUM CHLORIDE) SPRAY [PURETEK CORPORATION] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241004_a12715c0-77f2-7716-e053-2995a90a06d3.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 |
|---|
| 59088-315-16 | 59088031516 | 237 mL in 1 BOTTLE, SPRAY (59088-315-16) | 237 ml | 2020-03-18 | 0000-00-00 | No | No | Current |