FDA.reportPublic FDA data

Han-I-Foam

Product NDC
63533-855
Requested package NDC
63533-855-18
11-digit product format
635330855
Labeler code
63533
Product ID
63533-855_032b0f35-b441-434a-817c-6185a8b82158
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Momar Incorporated
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-08-10
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

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 · 7 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-04-01 02:39 UTC · source 2025-03-31IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
63533-855-082025-03-31Han-I-Foam 6585 Drug Facts and Label
63533-855-102025-03-31Han-I-Foam 6585 Drug Facts and Label
63533-855-112025-03-31Han-I-Foam 6585 Drug Facts and Label
63533-855-122025-03-31Han-I-Foam 6585 Drug Facts and Label
63533-855-142025-03-31Han-I-Foam 6585 Drug Facts and Label
63533-855-172025-03-31Han-I-Foam 6585 Drug Facts and Label
63533-855-182025-03-31Han-I-Foam 6585 Drug Facts and Label
63533-855-082025-01-30Han-I-Foam 6585 Drug Facts and Label
63533-855-102025-01-30Han-I-Foam 6585 Drug Facts and Label
63533-855-112025-01-30Han-I-Foam 6585 Drug Facts and Label
63533-855-122025-01-30Han-I-Foam 6585 Drug Facts and Label
63533-855-142025-01-30Han-I-Foam 6585 Drug Facts and Label
63533-855-172025-01-30Han-I-Foam 6585 Drug Facts and Label
63533-855-182025-01-30Han-I-Foam 6585 Drug Facts and Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90MHAN-I-FOAM (ALCOHOL) LIQUID [MOMAR INCORPORATED]1
ALCOHOLACTIVE MOIETY3K9958V90MHAN-I-FOAM (ALCOHOL) LIQUID [MOMAR INCORPORATED]1
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATEINACTIVE INGREDIENT4J55VM509SHAN-I-FOAM (ALCOHOL) LIQUID [MOMAR INCORPORATED]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3HAN-I-FOAM (ALCOHOL) LIQUID [MOMAR INCORPORATED]1
WATERINACTIVE INGREDIENT059QF0KO0RHAN-I-FOAM (ALCOHOL) LIQUID [MOMAR INCORPORATED]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63533-855-186353308551850 mL in 1 BOTTLE, PLASTIC (63533-855-18) 50 ml2020-08-100000-00-00NoNoCurrent