FDA.reportPublic FDA data

Fresh Wave IAQ Antiseptic Hand Rub

Product NDC
75399-014
11-digit product format
753990014
Labeler code
75399
Product ID
75399-014_ce8daed3-50cc-4ef7-8253-a5b0eb23829c
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
SOLUTION
Route
TOPICAL
Labeler
OMI Industries
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-04-15
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

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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct75399-014DDiscontinued by firm2026-07-31
excluded packagepackage75399-01475399-014-00DDiscontinued by firm2026-07-31

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75399-014-002021-07-26C16284748780-1c7ccaba7-1e5d-fd44-e053-dadaa90aa01b1cbd74a4-ccfb-4d3e-a7ed-528ccfa2a365
75399-014-002021-07-23C16284748780-1c7ccaba7-1e5d-fd44-e053-dadaa90aa01b1cbd74a4-ccfb-4d3e-a7ed-528ccfa2a365

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
75399-014-0075399001400236 mL in 1 BOTTLE, SPRAY (75399-014-00) 236 ml2020-04-150000-00-00NoNoCurrent