Hand Sanitizer

Product NDC
78553-4743
11-digit product format
785534743
Labeler code
78553
Product ID
78553-4743_f1723106-12ee-226c-e053-2a95a90af9a9
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
KIT
Route
TOPICAL
Labeler
Unitrex Ltd.
Application
Part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-11-06
Marketing end
2023-06-30
Active strength
0
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78553-4743-52023-01-04C16284748780-1e4f33bdf-9fdf-d8a0-e053-dadaa90a6e4eb58434b4-d730-2f17-e053-2995a90a9361
78553-4743-52022-07-29C16284748780-1e4f33bdf-9fdf-d8a0-e053-dadaa90a6e4eb58434b4-d730-2f17-e053-2995a90a9361

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
78553-4743-5785534743051 KIT in 1 KIT (78553-4743-5) * 15 mL in 1 BOTTLE, SPRAY (78553-4741-4) * 10 POUCH in 1 POUCH (78553-4742-2) > 70 mL in 1 POUCH1 kit2020-11-060000-00-00NoNoCurrent