NDC 21749-302 - PURELL Hand Sanitizing Wipes Clean Refreshing Scent

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 21749-302
Package NDCs from labels: 21749-302-10
Manufacturer: GOJO Industries, Inc.
Effective date: 2024-12-31
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
PURELL Hand Sanitizing Wipes Clean Refreshing Scent	GOJO Industries, Inc.	2024-12-31	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
21749-302-10	PURELL Hand Sanitizing Wipes Clean Refreshing Scent	10 in 1 PACKAGE	CLOTH	10		4
21749-302-10	PURELL Hand Sanitizing Wipes Clean Refreshing Scent	37 mL in 1 PACKAGE	CLOTH	37		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
21749-302	PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT (BENZALKONIUM CHLORIDE WIPE) CLOTH [GOJO INDUSTRIES, INC.]	4	2 package rows	20250101_6760ccd7-29c9-4df3-a6be-c7274be069bc.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 81 of 81 · 1,602 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sit Clean	BENZALKONIUM CHLORIDE	Sit Clean	ef2b12f8-89b3-47c4-88bd-8712a84cfc45	2016-08-18	Warnings	Exact identifier unii: F5UM2KM3W7
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.