Cleanslate

Product NDC
75601-1003
11-digit product format
756011003
Labeler code
75601
Product ID
75601-1003_d56f8533-e13a-048a-e053-2995a90afa20
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Punch Studio, LLC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-10-14
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
75 mL/100mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75601-1003-22023-07-28C16284748780-10191ceaa-6540-198a-e063-dbdaa90aec3eHand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75601-1003-1Cleanslate30 mL in 1 BOTTLE, SPRAYLIQUID305
75601-1003-2Cleanslate1 in 1 BOXLIQUID15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75601-1003CLEANSLATE (ALCOHOL) LIQUID [PUNCH STUDIO, LLC]5Legacy NDC, 2 package rows20220113_b1962c2d-ec29-e7c6-e053-2a95a90a0596.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1047755ethanol 75 % Topical SolutionPSNb1962c2d-ec29-e7c6-e053-2a95a90a05965
1047755ethanol 0.75 ML/ML Topical SolutionSCDb1962c2d-ec29-e7c6-e053-2a95a90a05965
1047755ethanol 75 % Topical SolutionSYb1962c2d-ec29-e7c6-e053-2a95a90a05965

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
75601-1003-17560110030130 mL in 1 BOTTLE, SPRAY30 mlHistorical
75601-1003-2756011003021 BOTTLE, SPRAY in 1 BOX (75601-1003-2) > 30 mL in 1 BOTTLE, SPRAY (75601-1003-1) 2020-10-140000-00-00NoNoCurrent