Kay Hand Sanitizer Foam
- Product NDC
- 47593-683
- 11-digit product format
- 475930683
- Labeler code
- 47593
- Product ID
- 47593-683_4f23f243-888d-4d54-98d0-e500946fe0f8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Ecolab Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-17
- Substance
- ALCOHOL
- Active strength
- 54.7 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Kay Hand Sanitizer Foam
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 54.7 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 1039465 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 47593-683-96 | Kay Hand Sanitizer Foam | 425 g in 1 CAN | SOLUTION | 425 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 47593-683-96 | 47593068396 | 425 g in 1 CAN (47593-683-96) | 425 g | 2025-12-17 | No | No | Current |