Alsoft W 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	59900-351	59900-351-07	I	Inactivated by FDA		2026-10-05

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

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59900-351-07	2026-01-29	C162847	48780-1	49896155-b006-586f-e063-e6dba90add90	Alsoft W 59900-351

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59900-351-07	Alsoft W hand sanitizer	500 mL in 1 BOTTLE	GEL	500		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59900-351	ALSOFT W HAND SANITIZER (ALCOHOL) GEL [BEST SANITIZERS, INC]	2	Legacy NDC, 1 package rows	20241218_b3ec9444-0fe0-6597-e053-2a95a90ac236.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3K9958V90M	ALCOHOL	64-17-5	ALCOHOL

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59900-351-07	59900035107	500 mL in 1 BOTTLE (59900-351-07)	500 ml	2020-10-30	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Alsoft W 59900-351	Best Sanitizers, Inc \| Best Sanitizers, Inc.	2024-12-05	HUMAN OTC DRUG LABEL	2