eZFoam Foaming Alcohol Hand Sanitizer

Product NDC
50865-688
Requested package NDC
50865-688-50
11-digit product format
508650688
Labeler code
50865
Product ID
50865-688_298e167d-7005-98da-e063-6294a90a07ba
Type
HUMAN OTC DRUG
Nonproprietary name
Foaming Hand Sanitizer
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Kutol Products Company
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2013-06-27
Substance
ALCOHOL
Active strength
62 mL/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 3 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage50865-68850865-688-50IInactivated by FDAexcluded / ndc_excluded.zipfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage50865-68850865-688-50IInactivated by FDAexcluded / ndc_excluded.zip86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage50865-68850865-688-50IInactivated by FDAexcluded / ndc_excluded.zipbd6a592717d7…303034d00443…

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
eZFoam Foaming Alcohol Hand Sanitizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL62 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
616763Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
1f56b4c5-d703-4193-83a8-3be815c8acdaAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50865-688-03eZFoam Foaming Alcohol Hand Sanitizer213125 mL in 1 DRUMSOLUTION2131256
50865-688-09eZFoam Foaming Alcohol Hand Sanitizer3785 mL in 1 JUGSOLUTION37856
50865-688-17eZFoam Foaming Alcohol Hand Sanitizer50 mL in 1 BOTTLE, PLASTICSOLUTION506
50865-688-24eZFoam Foaming Alcohol Hand Sanitizer1000 mL in 1 BAGSOLUTION10006
50865-688-41eZFoam Foaming Alcohol Hand Sanitizer1000 mL in 1 BAGSOLUTION10006
50865-688-50eZFoam Foaming Alcohol Hand Sanitizer1200 mL in 1 BAGSOLUTION12006
50865-688-78eZFoam Foaming Alcohol Hand Sanitizer950 mL in 1 BOTTLE, PLASTICSOLUTION9506
50865-688-91eZFoam Foaming Alcohol Hand Sanitizer532 mL in 1 BOTTLE, PLASTICSOLUTION5326

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50865-688EZFOAM FOAMING ALCOHOL HAND SANITIZER (FOAMING HAND SANITIZER) SOLUTION [KUTOL PRODUCTS COMPANY]6Current NDC, Legacy NDC, 8 package rows20241220_1f56b4c5-d703-4193-83a8-3be815c8acda.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
eZFoam Foaming Alcohol Hand SanitizerFOAMING HAND SANITIZERKutol Products Company1f56b4c5-d703-4193-83a8-3be815c8acda2024-12-18WarningsExact identifier
ndc (package): 50865-688-50
ndc (product): 50865-688
ndc11 (package): 50865068850

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
616763ethanol 62 % Topical FoamPSN1f56b4c5-d703-4193-83a8-3be815c8acda6
616763ethanol 0.62 ML/ML Topical FoamSCD1f56b4c5-d703-4193-83a8-3be815c8acda6
616763ethanol 62 % Topical FoamSY1f56b4c5-d703-4193-83a8-3be815c8acda6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50865-688-50508650688501200 mL in 1 BAG (50865-688-50) 1200 ml2013-06-270000-00-00NoNoCurrent