Liquid Wart Remover

Product NDC: 56104-245
11-digit product format: 561040245
Labeler code: 56104
Product ID: 56104-245_4097a58b-0d97-59ff-e063-6294a90a0252
Type: HUMAN OTC DRUG
Nonproprietary name: Salicylic Acid
Dosage form: LIQUID
Route: TOPICAL
Labeler: Premier Brands of America, Inc.
Application: M028
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-06-16
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: Liquid Wart Remover
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
e1964b8a-b5f1-32a6-e053-2a95a90a6e41	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
56104-245-01	Liquid Wart Remover	9 mL in 1 BOTTLE, WITH APPLICATOR	LIQUID	9		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
56104-245	LIQUID WART REMOVER (SALICYLIC ACID) LIQUID [PREMIER BRANDS OF AMERICA, INC.]	4	Current NDC, Legacy NDC, 1 package rows	20241013_e1964b8a-b5f1-32a6-e053-2a95a90a6e41.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
56104-245-01	56104024501	9 mL in 1 BOTTLE, WITH APPLICATOR (56104-245-01)	9 ml	2022-06-16	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Premier Solutions Liquid Wart Remover	Premier Brands of America, Inc.	2025-10-07	HUMAN OTC DRUG LABEL	5