Sani-Smooth

Product NDC
76063-773
11-digit product format
760630773
Labeler code
76063
Product ID
76063-773_658bf66d-8bcd-4e13-89fa-514b7259ea1e
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
Chromate Industrial Corporation
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-02-01
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
620 mg/g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76063-773-252019-10-29C16284748780-1960f7f55-cd07-8e05-e053-dbdaa90a074aSani-Smooth 4773 Drug Facts and Label
76063-773-262019-10-29C16284748780-1960f7f55-cd07-8e05-e053-dbdaa90a074aSani-Smooth 4773 Drug Facts and Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76063-773-25Sani-Smooth199 g in 1 CANAEROSOL, FOAM1991
76063-773-26Sani-Smooth454 g in 1 CANAEROSOL, FOAM4541

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76063-773SANI-SMOOTH (ALCOHOL) AEROSOL, FOAM [CHROMATE INDUSTRIAL CORPORATION]1Legacy NDC, 2 package rows20110405_622b1b39-579d-4a1d-958e-58f4b5783f2d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
616763ethanol 62 % Topical FoamPSN622b1b39-579d-4a1d-958e-58f4b5783f2d1
616763ethanol 0.62 ML/ML Topical FoamSCD622b1b39-579d-4a1d-958e-58f4b5783f2d1
616763ethanol 62 % Topical FoamSY622b1b39-579d-4a1d-958e-58f4b5783f2d1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
76063-773-2576063077325199 g in 1 CAN199 gHistorical
76063-773-2676063077326454 g in 1 CAN454 gHistorical