Foamitizer Foaming Hand Sanitizer

Product NDC
78166-800
11-digit product format
781660800
Labeler code
78166
Product ID
78166-800_84b1c06a-8f6e-467b-84a7-b20af3bea6ed
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Falcon Industrial, Inc.
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-07-01
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
80 L/100L
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78166-800-012022-01-28C16284748780-1d6a99b39-91ec-a426-e053-dadaa90af4c2e6d59e4d-d00e-4ccf-9f3a-a8bdade2225e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78166-800-01Foamitizer Foaming Hand Sanitizer3.785 L in 1 BOTTLESOLUTION3.7851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78166-800FOAMITIZER FOAMING HAND SANITIZER (ALCOHOL) SOLUTION [FALCON INDUSTRIAL, INC.]1Legacy NDC, 1 package rows20200728_e6d59e4d-d00e-4ccf-9f3a-a8bdade2225e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1663735ethanol 80 % Topical FoamPSNe6d59e4d-d00e-4ccf-9f3a-a8bdade2225e1
1663735ethanol 0.8 ML/ML Topical FoamSCDe6d59e4d-d00e-4ccf-9f3a-a8bdade2225e1
1663735ethanol 80 % Topical FoamSYe6d59e4d-d00e-4ccf-9f3a-a8bdade2225e1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
78166-800-01781660800013.785 L in 1 BOTTLE (78166-800-01) 3.785 l2020-07-010000-00-00NoNoCurrent