FDA.reportPublic FDA data

Foamahol

Product NDC
68654-855
Requested package NDC
68654-855-14
11-digit product format
686540855
Labeler code
68654
Product ID
68654-855_7a98da8b-ae38-4a6d-b2e1-5a198f11ffd0
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Share Corporation
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-07-11
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

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
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage68654-85568654-855-14UExcluded because listing certification expiredexcluded / ndc_excluded.zip302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage68654-85568654-855-14UExcluded because listing certification expiredexcluded / ndc_excluded.ziped331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage68654-85568654-855-14UExcluded because listing certification expiredexcluded / ndc_excluded.zip0efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68654-855-142025-02-01C16284748780-12cef2736-75ec-d83d-e063-dadaa90ab31fFoamahol 6585 Drug Facts and Label
68654-855-172025-02-01C16284748780-12cef2736-75ec-d83d-e063-dadaa90ab31fFoamahol 6585 Drug Facts and Label
68654-855-182025-02-01C16284748780-12cef2736-75ec-d83d-e063-dadaa90ab31fFoamahol 6585 Drug Facts and Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90MFOAMAHOL (ALCOHOL) LIQUID [SHARE CORPORATION]1
ALCOHOLACTIVE MOIETY3K9958V90MFOAMAHOL (ALCOHOL) LIQUID [SHARE CORPORATION]1
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATEINACTIVE INGREDIENT4J55VM509SFOAMAHOL (ALCOHOL) LIQUID [SHARE CORPORATION]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3FOAMAHOL (ALCOHOL) LIQUID [SHARE CORPORATION]1
WATERINACTIVE INGREDIENT059QF0KO0RFOAMAHOL (ALCOHOL) LIQUID [SHARE CORPORATION]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68654-855-14686540855143785 mL in 1 BOTTLE, PLASTIC (68654-855-14) 3785 ml2019-07-110000-00-00NoNoCurrent