FDA.reportPublic FDA data

Plantar Wart Removers

Product NDC
73469-6331
11-digit product format
734696331
Labeler code
73469
Product ID
73469-6331_467a8a9e-4812-2488-e063-6394a90ac5ec
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic acid
Dosage form
DISC
Route
TOPICAL
Labeler
Scholls Wellness Company LLC
Application
M028
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-05-23
Substance
SALICYLIC ACID
Active strength
.4 g/g
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
Plantar Wart Removers
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID.4 g/g

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
240559Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
fc9dc984-37c8-5bab-e053-6294a90a3c15Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73469-6331-2Plantar Wart Removers1 g in 1 POUCHDISC14
73469-6331-2Plantar Wart Removers12 in 1 CARTONDISC124

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73469-6331PLANTAR WART REMOVERS (SALICYLIC ACID) DISC [SCHOLLS WELLNESS COMPANY LLC]3Current NDC, 2 package rows20241006_fc9dc984-37c8-5bab-e053-6294a90a3c15.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
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
240559salicylic acid 40 % Medicated PatchPSNfc9dc984-37c8-5bab-e053-6294a90a3c154
240559salicylic acid 0.4 MG/MG Medicated PatchSCDfc9dc984-37c8-5bab-e053-6294a90a3c154
240559salicylic acid 40 % Medicated PatchSYfc9dc984-37c8-5bab-e053-6294a90a3c154

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
73469-6331-27346963310212 POUCH in 1 CARTON (73469-6331-2) / 1 g in 1 POUCH12 pouch2023-05-31NoNoCurrent