FIRST MARK ULTRA FOAMING ANTIBACTERIAL
- Product NDC
- 51042-001
- 11-digit product format
- 510420001
- Labeler code
- 51042
- Product ID
- 51042-001_f855444d-b8b3-4200-8ebe-481bb30ee25f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Performance Food Group
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-08-12
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 5 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
- FIRST MARK ULTRA FOAMING ANTIBACTERIAL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 5 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 |
|---|
| 51042-001-10 | FIRST MARK ULTRA FOAMING ANTIBACTERIAL | 1250 mL in 1 BOTTLE | SOLUTION | 1250 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51042-001 | FIRST MARK ULTRA FOAMING ANTIBACTERIAL (BENZALKONIUM CHLORIDE) SOLUTION [PERFORMANCE FOOD GROUP] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240807_968c0f18-d0b6-4f29-b001-00ac314a3bdd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51042-001-10 | 51042000110 | 1250 mL in 1 BOTTLE (51042-001-10) | 1250 ml | 2021-11-29 | 0000-00-00 | No | No | Current |