FDA.reportPublic FDA data

Greenex Hand Sanitizer

Product NDC
58575-202
Requested package NDC
58575-202-02
11-digit product format
585750202
Labeler code
58575
Product ID
58575-202_c0ed7011-e092-4d20-8ba2-5e1ad259f869
Type
HUMAN OTC DRUG
Nonproprietary name
Hand Sanitizer
Dosage form
LIQUID
Route
TOPICAL
Labeler
Inopak, Ltd
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-01-01
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage58575-20258575-202-02DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58575-202-02585750202026000 mL in 1 CASE (58575-202-02) 6000 ml2018-01-010000-00-00NoNoCurrent