FDA.reportPublic FDA data

Deb InstantFOAM Complete

Product NDC
11084-170
Requested package NDC
11084-170-40
11-digit product format
110840170
Labeler code
11084
Product ID
11084-170_754e345a-4954-4713-8711-64b05cd17857
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
LIQUID
Route
TOPICAL
Labeler
SC Johnson Professional USA, Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-08-18
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage11084-17011084-170-40DDiscontinued 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 · 9 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…

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 INGREDIENT3K9958V90MDEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1
ALCOHOLACTIVE MOIETY3K9958V90MDEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLDEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1
BIS-PEG-12 DIMETHICONE (500 MPA.S)INACTIVE INGREDIENT2CNS542YRTDEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1
COCO GLUCOSIDEINACTIVE INGREDIENTICS790225BDEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDEINACTIVE INGREDIENT0Y0NQR2GH1DEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1
GLYCERYL OLEATEINACTIVE INGREDIENT4PC054V79PDEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1
PANTHENOLINACTIVE INGREDIENTWV9CM0O67ZDEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1
PEG-200 HYDROGENATED GLYCERYL PALMATEINACTIVE INGREDIENTW161T051Y1DEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1
PEG-7 GLYCERYL COCOATEINACTIVE INGREDIENTVNX7251543DEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RDEB INSTANTFOAM COMPLETE (ALCOHOL) LIQUID [DEB USA, INC.]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11084-170-4011084017040400 mL in 1 BOTTLE, PLASTIC (11084-170-40) 400 ml2015-08-180000-00-00NoNoCurrent