Pure Force
- Product NDC
- 47593-504
- 11-digit product format
- 475930504
- Labeler code
- 47593
- Product ID
- 47593-504_02a396bc-771a-408b-9e39-12631092a9df
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Ecolab Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-10-28
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 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
- Pure Force
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1038799 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 47593-504-41 | Pure Force | 750 mL in 1 BOTTLE, PLASTIC | LIQUID | 750 | | 4 |
| 47593-504-59 | Pure Force | 1250 mL in 1 BOTTLE, PLASTIC | LIQUID | 1250 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 47593-504 | PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20240711_66fd73be-05c8-4905-96f5-f73fa1447b3f.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 |
|---|
| 47593-504-41 | 47593050441 | 750 mL in 1 BOTTLE, PLASTIC (47593-504-41) | 750 ml | 2013-10-28 | 0000-00-00 | No | No | Current |
| 47593-504-59 | 47593050459 | 1250 mL in 1 BOTTLE, PLASTIC | 1250 ml | | | | | Historical |