Pure Foam

Product NDC
50452-773
11-digit product format
504520773
Labeler code
50452
Product ID
50452-773_167bec9c-75c6-43ad-978b-b5862e435a7b
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
Phoenix Research Industries, Inc.
Application
part333
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2010-01-31
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
50452-773-252019-10-21C16284748780-1956f9ecf-bb7a-621f-e053-dbdaa90a74adPure Foam 4773 Drug Facts and Label
50452-773-262019-10-21C16284748780-1956f9ecf-bb7a-621f-e053-dbdaa90a74adPure Foam 4773 Drug Facts and Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50452-773-25Pure Foam199 g in 1 CANAEROSOL, FOAM1991
50452-773-26Pure Foam454 g in 1 CANAEROSOL, FOAM4541

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50452-773PURE FOAM (ALCOHOL) AEROSOL, FOAM [PHOENIX RESEARCH INDUSTRIES, INC.]1Legacy NDC, 2 package rows20100223_a2f9014c-0497-4be7-9e78-21506b4db8fd.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
616763ethanol 62 % Topical FoamPSNa2f9014c-0497-4be7-9e78-21506b4db8fd1
616763ethanol 0.62 ML/ML Topical FoamSCDa2f9014c-0497-4be7-9e78-21506b4db8fd1
616763ethanol 62 % Topical FoamSYa2f9014c-0497-4be7-9e78-21506b4db8fd1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
50452-773-2550452077325199 g in 1 CAN199 gHistorical
50452-773-2650452077326454 g in 1 CAN454 gHistorical