Mentholatum Moisturizing Hand Sanitizer
- Product NDC
- 10742-0004
- 11-digit product format
- 107420004
- Labeler code
- 10742
- Product ID
- 10742-0004_292b8cf3-73cf-8681-e063-6394a90abb04
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzalkonium chloride
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- The Mentholatum Company
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-06-12
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1.3 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
- Mentholatum Moisturizing Hand Sanitizer
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1.3 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1098199 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10742-0004-1 | Mentholatum Moisturizing Hand Sanitizer | 192 mL in 1 BOTTLE | GEL | 192 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10742-0004 | MENTHOLATUM MOISTURIZING HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [THE MENTHOLATUM COMPANY] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241215_365c93bc-2299-4e69-ba3a-69414bfe78d7.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 |
|---|
| 10742-0004-1 | 10742000401 | 192 mL in 1 BOTTLE (10742-0004-1) | 192 ml | 2020-06-12 | 0000-00-00 | No | No | Current |