HAND SANITIZER

Product NDC: 75023-003
11-digit product format: 750230003
Labeler code: 75023
Product ID: 75023-003_adca566b-e058-9c76-e053-2995a90aaf94
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: 1 L/1.893L
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
NDC	Effective	Action	Document	Indexing SPL	Related label
75023-003-04	2022-01-28	C162847	48780-1	d6a99b39-af33-a426-e053-dadaa90af4c2	VERSION 2: CORRECTION INTENDED TO REPLACE SETID SUBMISSION ENDING "..AB88E" CORRECTION: (1) BACK LABEL REPLACEMENT CONSUMER HAND SANITIZER; NON-EMERGENCY; ISOPROPYL ALCOHOL = DEFERRED GRASE ACTIVE INGREDIENT DETERMINATION EFFECTIVE APRIL 13, 2020; PART333E FOR OTC HAND RUB SANITIZERS (CONSUMER)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75023-003-04	HAND SANITIZER	1.893 L in 1 BOTTLE	LIQUID	1.893		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75023-003	HAND SANITIZER (ISOPROPYL ALCOHOL) LIQUID [SUN WAVE WELLNESS, LLC]	2	Legacy NDC, 1 package rows	20200827_a9b89b7a-e789-8afc-e053-2a95a90ab88e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Status
75023-003-04	75023000304	1.893 L in 1 BOTTLE	1.893 l	Historical