Numb 520

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	63742-002		I	Inactivated by FDA		2026-10-05
excluded package	package	63742-002	63742-002-01	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	Strength	SPL version
63742-002-01	Numb 520	38 g in 1 BOTTLE	CREAM	38		4
63742-002-01	Numb 520	1 in 1 PACKAGE	CREAM	1		4

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63742-002	NUMB 520 (LIDOCAINE) CREAM [CLINICAL RESOLUTION LABORATORY, INC.]	4	Legacy NDC, 2 package rows	20231227_f88829f2-d900-4b78-b2cc-eebd76c326cd.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
98PI200987	LIDOCAINE	137-58-6	LIDOCAINE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63742-002-01	63742000201	1 BOTTLE in 1 PACKAGE (63742-002-01) > 38 g in 1 BOTTLE	1 bottle	2015-12-18	0000-00-00	No	No	Current