Foaming Hand
- Product NDC
- 42961-224
- 11-digit product format
- 429610224
- Labeler code
- 42961
- Product ID
- 42961-224_49dac8e8-231b-6f18-e063-6394a90aecd1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Cintas Corporation
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-07-20
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1.3 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
- Foaming Hand
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1.3 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42961-224-71 | Foaming Hand | 800 mL in 1 BOTTLE, PUMP | LOTION | 800 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42961-224 | FOAMING HAND (BENZALKONIUM CHLORIDE) LOTION [CINTAS CORP] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250228_17fb34e7-c9e6-41aa-991f-bb54c84ed79c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42961-224-71 | 42961022471 | 800 mL in 1 BOTTLE, PUMP (42961-224-71) | 800 ml | 2020-07-20 | 0000-00-00 | No | No | Current |