Salicylic Acid

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	11822-0119		D	Discontinued by firm		2026-10-05
excluded package	package	11822-0119	11822-0119-9	D	Discontinued by firm		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
11822-0119-9	Salicylic Acid	9 mL in 1 BOTTLE, WITH APPLICATOR	LIQUID	9		9

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11822-0119	SALICYLIC ACID (LIQUID WART REMOVER) LIQUID [RITE AID CORPORATION]	8	Legacy NDC, 1 package rows	20241213_6f25036a-e55d-4be9-b090-f314b9b45760.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
O414PZ4LPZ	SALICYLIC ACID	69-72-7	SALICYLIC ACID

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11822-0119-9	11822011909	9 mL in 1 BOTTLE, WITH APPLICATOR (11822-0119-9)	9 ml	2017-12-22	0000-00-00	No	No	Current