FDA.reportPublic FDA data

HAND SANITIZER

Product NDC
75023-002
11-digit product format
750230002
Labeler code
75023
Product ID
75023-002_adcaed72-cd03-82d0-e053-2995a90a6d11
Type
HUMAN OTC DRUG
Nonproprietary name
ISOPROPYL ALCOHOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
SUN WAVE WELLNESS, LLC
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-07-05
Marketing end
0000-00-00
Substance
ISOPROPYL ALCOHOL
Active strength
70 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 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct75023-002IInactivated by FDA2026-07-31
excluded packagepackage75023-00275023-002-01IInactivated by FDA2026-07-31
excluded packagepackage75023-00275023-002-02IInactivated by FDA2026-07-31
excluded packagepackage75023-00275023-002-03IInactivated by FDA2026-07-31

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75023-002-012022-01-28C16284748780-1d6a99b39-e173-a426-e053-dadaa90af4c2VERSION 2: CORRECTION CORRECTION: (1) LABEL IMAGE CORRECTION CONSUMER HAND SANITIZER; NON-EMERGENCY; ISOPROPYL ALCHOL (IPA) = DEFERRED GRASE ACTIVE INGREDIENT DETERMINATION EFFECTIVE APRIL 13, 2020; PART333E FOR OTC HAND RUB SANTIZERS (CONSUMER)
75023-002-022022-01-28C16284748780-1d6a99b39-e173-a426-e053-dadaa90af4c2VERSION 2: CORRECTION CORRECTION: (1) LABEL IMAGE CORRECTION CONSUMER HAND SANITIZER; NON-EMERGENCY; ISOPROPYL ALCHOL (IPA) = DEFERRED GRASE ACTIVE INGREDIENT DETERMINATION EFFECTIVE APRIL 13, 2020; PART333E FOR OTC HAND RUB SANTIZERS (CONSUMER)
75023-002-032022-01-28C16284748780-1d6a99b39-e173-a426-e053-dadaa90af4c2VERSION 2: CORRECTION CORRECTION: (1) LABEL IMAGE CORRECTION CONSUMER HAND SANITIZER; NON-EMERGENCY; ISOPROPYL ALCHOL (IPA) = DEFERRED GRASE ACTIVE INGREDIENT DETERMINATION EFFECTIVE APRIL 13, 2020; PART333E FOR OTC HAND RUB SANTIZERS (CONSUMER)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75023-002-01HAND SANITIZER100 mL in 1 BOTTLE, SPRAYLIQUID1002
75023-002-02HAND SANITIZER100 mL in 1 BOTTLE, DISPENSINGLIQUID1002
75023-002-03HAND SANITIZER100 mL in 1 BOTTLE, WITH APPLICATORLIQUID1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75023-002HAND SANITIZER (ISOPROPYL ALCOHOL) LIQUID [SUN WAVE WELLNESS, LLC]2Legacy NDC, 3 package rows20200827_a9b5edf7-6837-ba04-e053-2995a90ac3e6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
75023-002-0175023000201100 mL in 1 BOTTLE, SPRAY100 mlHistorical
75023-002-0275023000202100 mL in 1 BOTTLE, DISPENSING100 mlHistorical
75023-002-0375023000203100 mL in 1 BOTTLE, WITH APPLICATOR100 mlHistorical