SSDC Foaming Hand Sanitizer
- Product NDC
- 47593-662
- 11-digit product format
- 475930662
- Labeler code
- 47593
- Product ID
- 47593-662_97346bba-3ef3-4124-945b-e3e331e474b7
- 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
- 2026-03-04
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SSDC Foaming Hand Sanitizer
- Listing expiration
- 2027-12-31
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 |
|---|
| 47593-662-70 | SSDC Foaming Hand Sanitizer | 1250 mL in 1 BOTTLE, PLASTIC | SOLUTION | 1250 | | 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 |
|---|
| 47593-662-70 | 47593066270 | 1250 mL in 1 BOTTLE, PLASTIC (47593-662-70) | 1250 ml | 2026-03-04 | No | No | Current |