Pureforce
- Product NDC
- 47593-473
- 11-digit product format
- 475930473
- Labeler code
- 47593
- Product ID
- 47593-473_43cdb212-385a-49ac-8119-2abf78c810eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Ecolab Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-04-27
- Marketing end
- 2026-07-06
- Substance
- ALCOHOL
- Active strength
- 60 mL/100mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pureforce
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 60 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 1039483 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 47593-473-25 | Pureforce | 800 mL in 1 POUCH | SOLUTION | 800 | | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 47593-473 | PUREFORCE (ALCOHOL) SOLUTION [ECOLAB INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20240426_09a88db3-2a8b-4752-96d8-6218203d4b45.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 |
|---|
| 47593-473-25 | 47593047325 | 800 mL in 1 POUCH (47593-473-25) | 800 ml | 2011-04-27 | 2026-07-06 | No | No | Current |