Hand Sanitizer

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

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

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	76370-0006	76370-0006-5	I	Inactivated by FDA		2026-10-05

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

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
76370-0006-1	Hand Sanitizer	3785 mL in 1 BOTTLE	LIQUID	3785	6
76370-0006-5	Hand Sanitizer	1000 mL in 1 BOTTLE, PLASTIC	LIQUID	1000	6
76370-0006-6	Hand Sanitizer	2400 mL in 1 BOTTLE, PLASTIC	LIQUID	2400	6

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76370-0006	HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [TAZZA BRANDS EAST INC.]	6	Legacy NDC, 3 package rows	20250124_464f97a0-623a-224f-e054-00144ff8d46c.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F5UM2KM3W7	BENZALKONIUM CHLORIDE	8001-54-5	BENZALKONIUM CHLORIDE

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1020365	benzalkonium chloride 0.13 % Topical Foam	PSN	464f97a0-623a-224f-e054-00144ff8d46c	6
1020365	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD	464f97a0-623a-224f-e054-00144ff8d46c	6
1020365	benzalkonium chloride 0.13 % Topical Foam	SY	464f97a0-623a-224f-e054-00144ff8d46c	6

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76370-0006-5	76370000605	1000 mL in 1 BOTTLE, PLASTIC (76370-0006-5)	1000 ml	2017-01-17	0000-00-00	No	No	Current