PureForce
- Product NDC
- 47593-568
- 11-digit product format
- 475930568
- Labeler code
- 47593
- Product ID
- 47593-568_b90a4807-6266-4fd8-a6c7-6f0e3597f937
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Ecolab Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-07-26
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 5 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
- PureForce
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1731737 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 47593-568-41 | PureForce | 750 mL in 1 BOTTLE, PLASTIC | SOLUTION | 750 | | 3 |
| 47593-568-59 | PureForce | 1250 mL in 1 BOTTLE, PLASTIC | SOLUTION | 1250 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 47593-568 | PUREFORCE (BENZALKONIUM CHLORIDE) SOLUTION [ECOLAB INC.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20240802_e624ea46-e502-4d2d-aaa1-59954f69be05.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 |
|---|
| 47593-568-41 | 47593056841 | 750 mL in 1 BOTTLE, PLASTIC (47593-568-41) | 750 ml | 2016-07-26 | 0000-00-00 | No | No | Current |
| 47593-568-59 | 47593056859 | 1250 mL in 1 BOTTLE, PLASTIC (47593-568-59) | 1250 ml | 2016-07-26 | 0000-00-00 | No | No | Current |