FDA.reportPublic FDA data

Han-I-Size

Product NDC
63533-221
11-digit product format
635330221
Labeler code
63533
Product ID
63533-221_2d0de76a-fd02-4900-8f0c-335e1d9af17b
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Momar Incorporated
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2005-12-01
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct63533-221DDiscontinued by firm2026-10-05
excluded packagepackage63533-22163533-221-14DDiscontinued by firm2026-10-05
excluded packagepackage63533-22163533-221-28DDiscontinued by firm2026-10-05

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
2025-12-14 17:58 UTC · source 2025-12-05excluded productproduct63533-221DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage63533-22163533-221-14DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage63533-22163533-221-28DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90MHAN-I-SIZE (ALCOHOL) GEL [MOMAR INCORPORATED]2
ALCOHOLACTIVE MOIETY3K9958V90MHAN-I-SIZE (ALCOHOL) GEL [MOMAR INCORPORATED]2
.ALPHA.-TOCOPHEROL ACETATE, DL-INACTIVE INGREDIENTWR1WPI7EW8HAN-I-SIZE (ALCOHOL) GEL [MOMAR INCORPORATED]2
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XHAN-I-SIZE (ALCOHOL) GEL [MOMAR INCORPORATED]2
CARBOMER 934INACTIVE INGREDIENTZ135WT9208HAN-I-SIZE (ALCOHOL) GEL [MOMAR INCORPORATED]2
DIISOPROPYLAMINEINACTIVE INGREDIENTBR9JLI40NOHAN-I-SIZE (ALCOHOL) GEL [MOMAR INCORPORATED]2
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3HAN-I-SIZE (ALCOHOL) GEL [MOMAR INCORPORATED]2
WATERINACTIVE INGREDIENT059QF0KO0RHAN-I-SIZE (ALCOHOL) GEL [MOMAR INCORPORATED]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63533-221HAN-I-SIZE (ALCOHOL) GEL [MOMAR INCORPORATED]4Legacy NDC20181227_3817bf34-c8fc-4dfe-a29f-14ba15ef11ed.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63533-221-14635330221143785 mL in 1 BOTTLE, PLASTIC (63533-221-14) 3785 ml2005-12-010000-00-00NoNoCurrent
63533-221-2863533022128149 mL in 1 BOTTLE, PLASTIC (63533-221-28) 149 ml2005-12-010000-00-00NoNoCurrent