FDA.reportPublic FDA data

Salicylic Acid

Product NDC
63868-299
11-digit product format
638680299
Labeler code
63868
Product ID
63868-299_53d7df48-ed3a-ad29-e063-6394a90a41e1
Type
HUMAN OTC DRUG
Nonproprietary name
Liquid Wart Remover
Dosage form
LIQUID
Route
TOPICAL
Labeler
Chain Drug Marketing Association Inc.
Application
M028
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2015-10-01
Marketing end
2027-09-30
Substance
SALICYLIC ACID
Active strength
.17 g/9mL
NDC exclude flag
No
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

Active Ingredients#

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

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

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
32bfbe17-21e9-4939-b4e0-fdf6acb56ef8Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63868-299-09Salicylic Acid9 mL in 1 BOTTLE, WITH APPLICATORLIQUID99

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63868-299-09ML - Milliliter63868-2990977bc19-ad5a-4495-a456-e8624df1210112022-10-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZSALICYLIC ACID (LIQUID WART REMOVER) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC.]1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZSALICYLIC ACID (LIQUID WART REMOVER) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC.]1
CAMPHOR (NATURAL)INACTIVE INGREDIENTN20HL7Q941SALICYLIC ACID (LIQUID WART REMOVER) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC.]1
CASTOR OILINACTIVE INGREDIENTD5340Y2I9GSALICYLIC ACID (LIQUID WART REMOVER) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC.]1
PYROXYLININACTIVE INGREDIENTKYR8BR2X6OSALICYLIC ACID (LIQUID WART REMOVER) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63868-299SALICYLIC ACID (LIQUID WART REMOVER) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC.]9Current NDC, Legacy NDC, 1 package rows20241213_32bfbe17-21e9-4939-b4e0-fdf6acb56ef8.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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63868-299-09638680299099 mL in 1 BOTTLE, WITH APPLICATOR (63868-299-09) 9 ml2015-10-012027-09-30NoNoCurrent