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

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
FIRST MARK ULTRA FOAMING ANTIBACTERIAL
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE5 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F5UM2KM3W7Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
968c0f18-d0b6-4f29-b001-00ac314a3bddAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51042-001-10FIRST MARK ULTRA FOAMING ANTIBACTERIAL1250 mL in 1 BOTTLESOLUTION12506

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51042-001FIRST MARK ULTRA FOAMING ANTIBACTERIAL (BENZALKONIUM CHLORIDE) SOLUTION [PERFORMANCE FOOD GROUP]4Current NDC, Legacy NDC, 1 package rows20240807_968c0f18-d0b6-4f29-b001-00ac314a3bdd.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FIRST MARK ULTRA FOAMING ANTIBACTERIALBENZALKONIUM CHLORIDEPerformance Food Group968c0f18-d0b6-4f29-b001-00ac314a3bdd2025-12-30WarningsExact identifier
ndc (product): 51042-001

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51042-001-10510420001101250 mL in 1 BOTTLE (51042-001-10) 1250 ml2021-11-290000-00-00NoNoCurrent