Uline Hand Sanitizer

Product NDC
69790-801
11-digit product format
697900801
Labeler code
69790
Product ID
69790-801_a7aa183f-8450-ff69-e053-2a95a90af0e0
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
Uline
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-06-08
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
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
69790-801-042024-10-01C16284748780-11030e365-06bb-111a-e063-dadaa90a10e2Uline Hand Sanitizer
69790-801-042024-07-30C16284748780-11030e365-06bb-111a-e063-dadaa90a10e2Uline Hand Sanitizer
69790-801-042024-01-30C16284748780-11030e365-06bb-111a-e063-dadaa90a10e2Uline Hand Sanitizer

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69790-801ULINE HAND SANITIZER (ALCOHOL) GEL [ULINE]2Legacy NDC20241225_a7aa3bde-d36e-f9d4-e053-2a95a90a6e6a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69790-801-04697900801043780 mL in 1 BOTTLE, PLASTIC (69790-801-04) 3780 ml2020-06-080000-00-00NoNoCurrent