COCA LIEF

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	84831-096		I	Inactivated by FDA		2026-09-14
excluded package	package	84831-096	84831-096-01	I	Inactivated by FDA		2026-09-14

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84831-096-01	COCA LIEF	100000 mg in 1 TUBE	GEL	100000		1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84831-096	COCA LIEF (MENTHOL, METHYLSALICYLATE) GEL [INDUSTRIA QUIMICO FARMACEUTICA SIGMA CORP. S.R.L.]	1	Current NDC, 1 package rows	20250120_2bedd2d0-b430-1844-e063-6294a90a965f.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
LAV5U5022Y	METHYL SALICYLATE	119-36-8	METHYL SALICYLATE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
84831-096-01	84831009601	100000 mg in 1 TUBE (84831-096-01)	100000 mg	2025-01-20	No	No	Historical