Salicylic Acid

Product NDC: 46122-362
11-digit product format: 461220362
Labeler code: 46122
Product ID: 46122-362_40976326-e3cf-25ce-e063-6294a90a9224
Type: HUMAN OTC DRUG
Nonproprietary name: Liquid Wart Remover
Dosage form: LIQUID
Route: TOPICAL
Labeler: AmerisourceBergen
Application: M028
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-07-01
Substance: SALICYLIC ACID
Active strength: .17 g/9mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Salicylic Acid
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SALICYLIC ACID	.17 g/9mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
O414PZ4LPZ	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5ac7242f-399a-4513-8932-90e5285ccb9f	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
46122-362-29	Salicylic Acid	9 mL in 1 BOTTLE, WITH APPLICATOR	LIQUID	9		9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
46122-362-29	ML - Milliliter	46122-362	cdf2231b-986b-437d-bbdd-43604971e28e	1	2017-03-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
46122-362	SALICYLIC ACID (LIQUID WART REMOVER) LIQUID [AMERISOURCEBERGEN DRUG CORPORATION]	7	Current NDC, Legacy NDC, 1 package rows	20241123_5ac7242f-399a-4513-8932-90e5285ccb9f.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 16 of 16 · 305 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ulensy Corn Callus and Wart Remover	CORN CALLUS AND WART REMOVER	Shenzhen Xinxin Yunhai Technology Co., Ltd.	0f3353ef-e105-7bd4-e063-6394a90a2562	2024-01-18	Warnings	Exact identifier application number: M028
WARTRIN Wart Remover	SALICYLIC ACID	BALBOA COMPANIES LLC	62c99f48-3dc1-4b41-8bc4-e93e2decadd9	2023-11-11	Warnings	Exact identifier application number: M028
UFORIC Wart Remover	SALICYLIC ACID	UFORIC HEALTH LLC	0d06cac6-5296-4d8a-b59e-966baac6be5f	2023-11-06	Warnings	Exact identifier application number: M028
WARTOVIR Wart Remover	SALICYLIC ACID	BALBOA COMPANIES LLC	2dbf5b40-d759-4c37-8dfe-3b65a7e6dbb6	2023-11-06	Warnings	Exact identifier application number: M028
VerruStat Wart Remover	SALICYLIC ACID	Clinical Therapeutic Solutions	16607d6e-6a5f-4b03-b38c-3610aef9b165	2023-11-05	Warnings	Exact identifier application number: M028

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
46122-362-29	46122036229	9 mL in 1 BOTTLE, WITH APPLICATOR (46122-362-29)	9 ml	2016-07-01	0000-00-00	No	No	Current