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

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 HAND SANITIZER
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL60 mL/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3K9958V90MInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1039483Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
80a490b4-dae5-4851-b3e6-2e558cdc51e5Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51042-002-09FIRST MARK ULTRA HAND SANITIZER1200 mL in 1 BOTTLE, PLASTICLIQUID12006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51042-002FIRST MARK ULTRA HAND SANITIZER (ALCOHOL) LIQUID [PERFORMANCE FOOD GROUP]4Current NDC, Legacy NDC, 1 package rows20240807_80a490b4-dae5-4851-b3e6-2e558cdc51e5.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 HAND SANITIZERALCOHOLPerformance Food Group80a490b4-dae5-4851-b3e6-2e558cdc51e52025-12-30WarningsExact identifier
ndc (product): 51042-002

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1039483ethanol 60 % Topical SolutionPSN80a490b4-dae5-4851-b3e6-2e558cdc51e56
1039483ethanol 0.6 ML/ML Topical SolutionSCD80a490b4-dae5-4851-b3e6-2e558cdc51e56
1039483ethanol 60 % Topical SolutionSY80a490b4-dae5-4851-b3e6-2e558cdc51e56

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51042-002-09510420002091200 mL in 1 BOTTLE, PLASTIC (51042-002-09) 1200 ml2021-05-210000-00-00NoNoCurrent