CANDO Ultra Hand Sanitizer

Product NDC
51452-108
11-digit product format
514520108
Labeler code
51452
Product ID
51452-108_b069b772-568c-6560-e053-2995a90a5691
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Fabrication Enterprises
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-09-29
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
70 mL/100mL
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
51452-108-012024-01-30C16284748780-11030e364-fe7c-111a-e063-dadaa90a10e2CANDO Ultra Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51452-108-01CANDO Ultra Hand Sanitizer236 mL in 1 BOTTLE, PUMPGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51452-108CANDO ULTRA HAND SANITIZER (ALCOHOL) GEL [FABRICATION ENTERPRISES]1Legacy NDC, 1 package rows20200929_b06a13fb-eb6f-2222-e053-2995a90afca4.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSNb06a13fb-eb6f-2222-e053-2995a90afca41
581662ethanol 0.7 ML/ML Topical GelSCDb06a13fb-eb6f-2222-e053-2995a90afca41
581662ethanol 70 % Topical GelSYb06a13fb-eb6f-2222-e053-2995a90afca41
581662ethyl alcohol 70 % Topical GelSYb06a13fb-eb6f-2222-e053-2995a90afca41

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51452-108-0151452010801236 mL in 1 BOTTLE, PUMP (51452-108-01) 236 ml2020-09-290000-00-00NoNoCurrent