FIRST MARK ULTRA HAND SANITIZER
- Product NDC
- 51042-002
- 11-digit product format
- 510420002
- Labeler code
- 51042
- Product ID
- 51042-002_062191ee-42af-4727-bdef-95cb62f5dd3b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Performance Food Group
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-05-21
- Substance
- ALCOHOL
- Active strength
- 60 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FIRST MARK ULTRA HAND SANITIZER
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 60 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 1039483 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51042-002-09 | FIRST MARK ULTRA HAND SANITIZER | 1200 mL in 1 BOTTLE, PLASTIC | LIQUID | 1200 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51042-002 | FIRST MARK ULTRA HAND SANITIZER (ALCOHOL) LIQUID [PERFORMANCE FOOD GROUP] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240807_80a490b4-dae5-4851-b3e6-2e558cdc51e5.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 |
|---|
| 51042-002-09 | 51042000209 | 1200 mL in 1 BOTTLE, PLASTIC (51042-002-09) | 1200 ml | 2021-05-21 | 0000-00-00 | No | No | Current |