Foaming Sanitizing Hand

Product NDC
50865-710
Requested package NDC
50865-710-55
11-digit product format
508650710
Labeler code
50865
Product ID
50865-710_50375794-9187-674e-e063-6394a90a6dff
Type
HUMAN OTC DRUG
Nonproprietary name
alcohol
Dosage form
SOAP
Route
TOPICAL
Labeler
Kutol Products Company
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2015-10-01
Substance
ALCOHOL
Active strength
.072 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
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 · 4 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2022-08-30 03:57 UTC · source 2022-08-29fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-0886f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01bd6a592717d7…303034d00443…
2021-12-27 23:28 UTC · source 2021-12-278dfbde2a14a4…c9ff85d89658…

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
Foaming Sanitizing Hand
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL.072 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

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

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
b2e22e51-88f5-4391-8705-3855c1645d80Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
50865-710-172023-08-18Kutol F710F
50865-710-412023-08-18Kutol F710F
50865-710-442023-08-18Kutol F710F
50865-710-552023-08-18Kutol F710F
50865-710-912023-08-18Kutol F710F
50865-710-172021-01-29Kutol F710F
50865-710-412021-01-29Kutol F710F
50865-710-442021-01-29Kutol F710F
50865-710-552021-01-29Kutol F710F
50865-710-912021-01-29Kutol F710F

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50865-710-17Foaming Sanitizing Hand50 mL in 1 BOTTLE, PLASTICSOAP509
50865-710-41Foaming Sanitizing Hand1000 mL in 1 BAGSOAP10009
50865-710-44Foaming Sanitizing Hand1000 mL in 1 BAGSOAP10009
50865-710-55Foaming Sanitizing Hand1200 mL in 1 BAGSOAP12009
50865-710-91Foaming Sanitizing Hand532 mL in 1 BOTTLE, PUMPSOAP5329
50865-710-92Foaming Sanitizing Hand59 mL in 1 BOTTLESOAP599

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50865-710FOAMING SANITIZING HAND (ALCOHOL) SOAP [KUTOL PRODUCTS COMPANY]8Current NDC, Legacy NDC, 6 package rows20241220_b2e22e51-88f5-4391-8705-3855c1645d80.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
Foaming Sanitizing HandALCOHOLKutol Products Companyb2e22e51-88f5-4391-8705-3855c1645d802026-04-24WarningsExact identifier
ndc (package): 50865-710-55
ndc (product): 50865-710
ndc11 (package): 50865071055

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
50865-710-55508650710551200 mL in 1 BAG (50865-710-55) 1200 ml2015-10-01NoNoCurrent