FDA.reportPublic FDA data

SANIFOAM HAND SANITIZER

Product NDC
50536-039
Requested package NDC
50536-039-01
11-digit product format
505360039
Labeler code
50536
Product ID
50536-039_d5a5b288-b9a7-eeda-e053-2a95a90a1869
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
LOTION
Route
TOPICAL
Labeler
AMERICAN CHEMICAL AND SANITARY SUPPLY INC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-03-12
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
62 mL/100mL
NDC exclude flag
No
Listing certified through
2023-12-31
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 packagepackage50536-03950536-039-01IInactivated by FDA2026-10-16

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 · 1 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
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage50536-03950536-039-01IInactivated by FDAexcluded / ndc_excluded.zip1332a3947898…d4bfe170f9cd…

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
50536-039-012024-05-09C16284748780-11030e365-2e2e-111a-e063-dadaa90a10e2AMERICAN CHEMICAL AND SANITARY SUPPLY - SANIFOAM HAND SANITIZER (50536-039)
50536-039-012024-01-30C16284748780-11030e365-2e2e-111a-e063-dadaa90a10e2AMERICAN CHEMICAL AND SANITARY SUPPLY - SANIFOAM HAND SANITIZER (50536-039)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50536-039-01SANIFOAM HAND SANITIZER3785 mL in 1 JUGLOTION37858

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90MSANIFOAM HAND SANITIZER (ALCOHOL) LOTION [AMERICAN CHEMICAL AND SANITARY SUPPLY INC]4
ALCOHOLACTIVE MOIETY3K9958V90MSANIFOAM HAND SANITIZER (ALCOHOL) LOTION [AMERICAN CHEMICAL AND SANITARY SUPPLY INC]4
WATERINACTIVE INGREDIENT059QF0KO0RSANIFOAM HAND SANITIZER (ALCOHOL) LOTION [AMERICAN CHEMICAL AND SANITARY SUPPLY INC]4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50536-039SANIFOAM HAND SANITIZER (ALCOHOL) LOTION [AMERICAN CHEMICAL AND SANITARY SUPPLY INC]8Legacy NDC, 1 package rows20240511_9879a4c2-28d7-410f-b895-2a43dad684c2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1491773alcohol 62 % Medicated Liquid SoapPSN9879a4c2-28d7-410f-b895-2a43dad684c28
1491773ethanol 0.62 ML/ML Medicated Liquid SoapSCD9879a4c2-28d7-410f-b895-2a43dad684c28
1491773ethanol 62 % Medicated Liquid SoapSY9879a4c2-28d7-410f-b895-2a43dad684c28

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50536-039-01505360039013785 mL in 1 JUG (50536-039-01) 3785 ml2014-03-120000-00-00NoNoCurrent