FDA.reportPublic FDA data

Compound W

Product NDC
63029-592
11-digit product format
630290592
Labeler code
63029
Product ID
63029-592_699aeaf0-6549-4299-8e1e-319e38af0770
Type
HUMAN OTC DRUG
Nonproprietary name
salicylic acid
Dosage form
LIQUID
Route
TOPICAL
Labeler
Medtech Products Inc.
Application
M028
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2014-03-01
Substance
SALICYLIC ACID
Active strength
.17 g/9g
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
Compound W
Brand name suffix
Maximum Strength Fast Acting Liquid
Listing expiration
2027-12-31

Active Ingredients#

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

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
70ca420d-b491-4f47-a994-374769619352Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63029-592-09Compound WMaximum Strength Fast Acting Liquid1 in 1 CARTONLIQUID13
63029-592-09Compound WMaximum Strength Fast Acting Liquid9 g in 1 BOTTLE, WITH APPLICATORLIQUID93

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63029-592COMPOUND W MAXIMUM STRENGTH FAST ACTING LIQUID (SALICYLIC ACID) LIQUID [MEDTECH PRODUCTS INC.]2Current NDC, 2 package rows20241101_70ca420d-b491-4f47-a994-374769619352.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 formatDescriptionMarketing startSampleExclude flagStatus
63029-592-09630290592091 BOTTLE, WITH APPLICATOR in 1 CARTON (63029-592-09) / 9 g in 1 BOTTLE, WITH APPLICATOR2014-03-01NoNoCurrent