KLEENFOAM

Product NDC
61924-093
11-digit product format
619240093
Labeler code
61924
Product ID
61924-093_9c5944f3-939d-b174-e053-2995a90ac030
Type
HUMAN OTC DRUG
Nonproprietary name
OTC ANTIMICROBIAL DRUG PRODUCT
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
Dermarite Industries LLC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-12-12
Marketing end
0000-00-00
Substance
CHLOROXYLENOL
Active strength
0 g/mL
NDC exclude flag
No
Listing certified through
2021-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct61924-093IInactivated by FDA2026-10-05
excluded packagepackage61924-09361924-093-34IInactivated by FDA2026-10-05

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 · 18 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage61924-093-34ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage61924-093-34367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage61924-093-34557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28excluded productproduct8af77b9d5b6f…d9bbb34c5368…
2024-05-28 21:12 UTC · source 2024-05-28excluded packagepackage61924-093-348af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14excluded productproduct834df4deac94…adcc014656a3…
2024-05-15 03:39 UTC · source 2024-05-14excluded packagepackage61924-093-34834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08excluded productproduct1332a3947898…d4bfe170f9cd…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage61924-093-341332a3947898…d4bfe170f9cd…
2022-08-30 03:57 UTC · source 2022-08-29excluded productproductfb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage61924-093-34fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproduct86f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage61924-093-3486f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproductbd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage61924-093-34bd6a592717d7…303034d00443…

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
61924-093-342024-12-06C16284748780-1d6a99b39-51c5-a426-e053-dadaa90af4c2DRUG LISTING: KLEENFOAM
61924-093-342022-01-28C16284748780-1d6a99b39-51c5-a426-e053-dadaa90af4c2DRUG LISTING: KLEENFOAM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61924-093-34KLEENFOAM1000 mL in 1 CARTRIDGEAEROSOL, FOAM10007

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ChloroxylenolACTIVE INGREDIENT0F32U78V2QKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
CHLOROXYLENOLACTIVE MOIETY0F32U78V2QKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
Cocamidopropyl BetaineINACTIVE INGREDIENT5OCF3O11KXKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
COCO MONOETHANOLAMIDEINACTIVE INGREDIENTC80684146DKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
DMDM HydantoinINACTIVE INGREDIENTBYR0546TOWKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
EDETATE SODIUMINACTIVE INGREDIENTMP1J8420LUKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
LEMON OILINACTIVE INGREDIENTI9GRO824LLKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
MethylchloroisothiazolinoneINACTIVE INGREDIENTDEL7T5QRPNKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
MethylisothiazolinoneINACTIVE INGREDIENT229D0E1QFAKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9TKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
POLYSORBATE 20INACTIVE INGREDIENT7T1F30V5YHKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
Propylene GlycolINACTIVE INGREDIENT6DC9Q167V3KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OHKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
Sodium HydroxideINACTIVE INGREDIENT55X04QC32IKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
SODIUM ISOSTEAROYL LACTYLATEINACTIVE INGREDIENT8730J0D3EVKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
Sodium Laureth SulfateINACTIVE INGREDIENTBPV390UAP0KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
Sodium Lauryl SulfateINACTIVE INGREDIENT368GB5141JKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
WATERINACTIVE INGREDIENT059QF0KO0RKLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61924-093KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]7Legacy NDC, 1 package rows20241208_f4ea9ae8-c783-48b4-af31-a26ecaa34992.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1550947chloroxylenol 0.5 % Topical FoamPSNf4ea9ae8-c783-48b4-af31-a26ecaa349927
1550947chloroxylenol 5 MG/ML Topical FoamSCDf4ea9ae8-c783-48b4-af31-a26ecaa349927
1550947chloroxylenol 0.5 % Topical FoamSYf4ea9ae8-c783-48b4-af31-a26ecaa349927

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61924-093-34619240093341000 mL in 1 CARTRIDGE (61924-093-34) 1000 ml2011-12-120000-00-00NoNoCurrent