FDA.reportPublic FDA data

SootheSense Wart Remover Liquid

Product NDC
76986-028
11-digit product format
769860028
Labeler code
76986
Product ID
76986-028_4f15b956-3cdb-21f3-e063-6394a90ab0f2
Type
HUMAN OTC DRUG
Nonproprietary name
SALICYLIC ACID
Dosage form
LIQUID
Route
TOPICAL
Labeler
Guangdong Quadrant Ecological Technology Co., Ltd.
Application
M028
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-03-10
Substance
SALICYLIC ACID
Active strength
.17 g/mL
NDC exclude flag
No
Listing certified through
2027-12-31
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
SootheSense Wart Remover Liquid
Listing expiration
2027-12-31

Active Ingredients#

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O414PZ4LPZInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
312881Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
4ca4361c-3c9a-e095-e063-6394a90ac456Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76986-028-01SootheSense Wart Remover Liquid30 mL in 1 BOTTLELIQUID302
76986-028-02SootheSense Wart Remover Liquid4 mL in 1 BOTTLELIQUID42
76986-028-02SootheSense Wart Remover Liquid3 in 1 BOXLIQUID32

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ulensy Corn Callus and Wart RemoverCORN CALLUS AND WART REMOVERShenzhen Xinxin Yunhai Technology Co., Ltd.0f3353ef-e105-7bd4-e063-6394a90a25622024-01-18WarningsExact identifier
application number: M028
WARTRIN Wart RemoverSALICYLIC ACIDBALBOA COMPANIES LLC62c99f48-3dc1-4b41-8bc4-e93e2decadd92023-11-11WarningsExact identifier
application number: M028
UFORIC Wart RemoverSALICYLIC ACIDUFORIC HEALTH LLC0d06cac6-5296-4d8a-b59e-966baac6be5f2023-11-06WarningsExact identifier
application number: M028
WARTOVIR Wart RemoverSALICYLIC ACIDBALBOA COMPANIES LLC2dbf5b40-d759-4c37-8dfe-3b65a7e6dbb62023-11-06WarningsExact identifier
application number: M028
VerruStat Wart RemoverSALICYLIC ACIDClinical Therapeutic Solutions16607d6e-6a5f-4b03-b38c-3610aef9b1652023-11-05WarningsExact identifier
application number: M028

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312881salicylic acid 17 % Topical SolutionPSN4ca4361c-3c9a-e095-e063-6394a90ac4562
312881salicylic acid 170 MG/ML Topical SolutionSCD4ca4361c-3c9a-e095-e063-6394a90ac4562
312881salicylic acid 17 % Topical SolutionSY4ca4361c-3c9a-e095-e063-6394a90ac4562

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
76986-028-017698600280130 mL in 1 BOTTLE (76986-028-01) 30 ml2026-03-10NoNoCurrent
76986-028-02769860028023 BOTTLE in 1 BOX (76986-028-02) / 4 mL in 1 BOTTLE3 bottle2026-03-10NoNoCurrent