Hand Sanitizer

Product NDC
79516-4934
11-digit product format
795164934
Labeler code
79516
Product ID
79516-4934_aaf6247d-8271-05ae-e053-2a95a90afbc0
Type
HUMAN OTC DRUG
Nonproprietary name
WHO recommended hand rub
Dosage form
LIQUID
Route
TOPICAL
Labeler
One Sanitizer, LLC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-03-30
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
80 mL/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79516-4934-1Hand Sanitizer120 mL in 1 BOTTLE, SPRAYLIQUID1202
79516-4934-2Hand Sanitizer1893 mL in 1 BOTTLE, SPRAYLIQUID18932
79516-4934-3Hand Sanitizer3785 mL in 1 BOTTLE, SPRAYLIQUID37852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79516-4934HAND SANITIZER (ALCOHOL) GEL HAND SANITIZER (WHO RECOMMENDED HAND RUB) LIQUID [ONE SANITIZER, LLC]2Legacy NDC, 3 package rows20200722_a7aa183f-8437-ff69-e053-2a95a90af0e0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1041498ethanol 80 % Topical GelPSNa7aa183f-8437-ff69-e053-2a95a90af0e02
1041498ethanol 0.8 ML/ML Topical GelSCDa7aa183f-8437-ff69-e053-2a95a90af0e02
1041498ethanol 80 % Topical GelSYa7aa183f-8437-ff69-e053-2a95a90af0e02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79516-4934-179516493401120 mL in 1 BOTTLE, SPRAY (79516-4934-1) 120 ml2020-03-300000-00-00NoNoCurrent
79516-4934-2795164934021893 mL in 1 BOTTLE, SPRAY (79516-4934-2) 1893 ml2020-03-300000-00-00NoNoCurrent
79516-4934-3795164934033785 mL in 1 BOTTLE, SPRAY (79516-4934-3) 3785 ml2020-03-300000-00-00NoNoCurrent