EELHOE Skin Tags Remove

Product NDC: 85064-015
11-digit product format: 850640015
Labeler code: 85064
Product ID: 85064-015_448e4bb4-1315-3858-e063-6294a90aef13
Type: HUMAN OTC DRUG
Nonproprietary name: SALICYLIC ACID
Dosage form: LIQUID
Route: TOPICAL
Labeler: Shantou Eelhoe Daily Chemical Technology Co., Ltd.
Application: M028
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-10-30
Substance: GINKGO BILOBA LEAF; PHELLODENDRON AMURENSE BARK; COIX LACRYMA-JOBI MA-YUEN SEED; SOPHORA FLAVESCENS ROOT
Active strength: .003; .003; .003; .003 mg/3mg; mg/3mg; mg/3mg; mg/3mg
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: EELHOE Skin Tags Remove
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
GINKGO BILOBA LEAF	.003 mg/3mg
PHELLODENDRON AMURENSE BARK	.003 mg/3mg
COIX LACRYMA-JOBI MA-YUEN SEED	.003 mg/3mg
SOPHORA FLAVESCENS ROOT	.003 mg/3mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
19FUJ2C58T	Internal UNII lookup
PBG27B754G	Internal UNII lookup
8DW238I7ZI	Internal UNII lookup
IYR6K8KQ5K	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
425b48fd-7be7-58ad-e063-6294a90a0773	Available on FDA.report

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85064-015-01	EELHOE Skin Tags Remove	3 mg in 1 BOX	LIQUID	3		2

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
PBG27B754G	PHELLODENDRON AMURENSE BARK		PHELLODENDRON AMURENSE BARK
IYR6K8KQ5K	SOPHORA FLAVESCENS ROOT		SOPHORA FLAVESCENS ROOT
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	Sample	Exclude flag	Status
85064-015-01	85064001501	3 mg in 1 BOX (85064-015-01)	3 mg	2025-10-30	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
EELHOE Skin Tags Remove - Shantou Eelhoe Daily Chemical Technology Co., Ltd.	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	2025-11-27	HUMAN OTC DRUG LABEL	2