FDA.reportPublic FDA data

SAN-E-FOAM

Product NDC
61924-107
Requested package NDC
61924-107-17
11-digit product format
619240107
Labeler code
61924
Product ID
61924-107_9c597550-4b74-876f-e053-2a95a90af2d8
Type
HUMAN OTC DRUG
Nonproprietary name
OTC ANTIMICROBIAL DRUG PRODUCTS
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
Dermarite Industries LLC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2012-10-12
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage61924-10761924-107-17IInactivated 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 · 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
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-288af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…
2022-08-30 03:57 UTC · source 2022-08-29fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-0886f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01bd6a592717d7…303034d00443…

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
61924-107-172026-01-29DRUG LISTING: SAN-E-FOAM
61924-107-342026-01-29DRUG LISTING: SAN-E-FOAM
61924-107-172024-12-06DRUG LISTING: SAN-E-FOAM
61924-107-342024-12-06DRUG LISTING: SAN-E-FOAM
61924-107-172022-01-28DRUG LISTING: SAN-E-FOAM
61924-107-342022-01-28DRUG LISTING: SAN-E-FOAM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61924-107-17SAN-E-FOAM50 mL in 1 BOTTLE, PUMPAEROSOL, FOAM507
61924-107-34SAN-E-FOAM1000 mL in 1 CARTRIDGEAEROSOL, FOAM10007

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90MSAN-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
ALCOHOLACTIVE MOIETY3K9958V90MSAN-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
.ALPHA.-TOCOPHEROL ACETATEINACTIVE INGREDIENT9E8X80D2L0SAN-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
GlycerinINACTIVE INGREDIENTPDC6A3C0OXSAN-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
PEG-10 DIMETHICONE (600 CST)INACTIVE INGREDIENT8PR7V1SVM0SAN-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3
WATERINACTIVE INGREDIENT059QF0KO0RSAN-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61924-107SAN-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC]7Legacy NDC, 2 package rows20241208_4c4bcbad-5c83-459f-8775-dc7bef8ad501.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1041847ethanol 67 % Topical FoamPSN4c4bcbad-5c83-459f-8775-dc7bef8ad5017
1041847ethanol 0.67 ML/ML Topical FoamSCD4c4bcbad-5c83-459f-8775-dc7bef8ad5017
1041847ethanol 67 % Topical FoamSY4c4bcbad-5c83-459f-8775-dc7bef8ad5017

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61924-107-176192401071750 mL in 1 BOTTLE, PUMP (61924-107-17) 50 ml2012-10-120000-00-00NoNoCurrent