Compound W Total Care Wart and Skin Kit

Product NDC
49354-130
11-digit product format
493540130
Labeler code
49354
Product ID
49354-130_08bf29ff-1c69-1547-e063-6294a90ac7ee
Type
HUMAN OTC DRUG
Nonproprietary name
SALICYLIC ACID
Dosage form
KIT
Labeler
HK Kolmar Canada, Inc
Application
M032
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-12-05
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
Compound W Total Care Wart and Skin Kit
Listing expiration
2026-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
210140Internal RxNorm lookup
312880Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
def46762-990a-48b0-b702-15ece1dc541fAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49354-003-00Compound W Total Care Wart and Skin Kit7 g in 1 TUBEGEL7 g170 mg in 1g2
49354-003-00Compound W Total Care Wart and Skin Kit1 in 1 CARTONGEL170 mg in 1g2
49354-130-00Compound W Total Care Wart and Skin Kit1 in 1 KITKIT12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49354-130COMPOUND W TOTAL CARE WART AND SKIN KIT (SALICYLIC ACID) KIT [HK KOLMAR CANADA, INC]2Current NDC, Legacy NDC, 3 package rows20231030_def46762-990a-48b0-b702-15ece1dc541f.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 31 of 31 · 613 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Glovers Medicated Anti-Dandruff ScalpSALICYLIC ACIDJ. Strickland & Co.bdf40a16-7b40-497e-939d-366cbe62b5552023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Original Anti-Dandruff Hair and Scalp ConditionerSULFURJ. Strickland & Co.eb1d6e9e-e7fd-478e-80c0-3a3f529682d72023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Loc Twist and Braid ScalpSALICYLIC ACIDJ. Strickland & Co.1aee59aa-ed8e-4f95-be99-63ce0814c03c2023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Fresh Anti-Dandruff Hair and Scalp ConditionerSALICYLIC ACIDJ. Strickland & Co.27b6276a-eaa0-4fb7-996c-53e8c28680912023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff ControlSALICYLIC ACIDJ. Strickland and Co.961ffab9-4e1b-83f3-e053-2a95a90af5fe2023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing TreatmentSALICYLIC ACIDJ. Strickland and Co.96b24a6f-3d6e-6d60-e053-2a95a90a83302023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Oil SerumSULFURJ. Strickland and Co.96b249a2-3f50-1ab8-e053-2995a90a56ed2023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Butter CreamSULFUR, SALICYLIC ACIDJ. Strickland and Co.96b26d20-d4d8-1bc3-e053-2995a90afec02023-10-21WarningsExact identifier
application number: M032
Glovers Clinical Care Seborrheic Dermatitis AntidandruffPYRITHIONE ZINCJ. Strickland and Co.fef5701f-c5c7-4932-9a1c-42532e3910a52023-10-21WarningsExact identifier
application number: M032
Topco AssociatesSELENIUM SULFIDETopco Associatesecf87660-f552-1f6b-e053-2a95a90a24862023-05-04WarningsExact identifier
application number: M032
Careone Medicated DandruffSELENIUM SULFIDERetail Business Services, LLCcb05b9c6-c1bb-b210-e053-2a95a90afaea2021-08-26WarningsExact identifier
application number: M032
GoodSense Medicated Dandruff Anti-Seborrheic Dermatitis, Anti-DandruffSELENIUM SULFIDEGOODSENSE21291e29-57ab-4761-8e8c-eef43ca65b242020-06-30WarningsExact identifier
application number: M032
ZolidynePYRITHIONE ZINCTopiderm, Inc.6d5eaecc-a3a1-4739-ae5b-66df4a15cd212019-11-20WarningsExact identifier
application number: M032

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
210140Compound W 17 % Topical GelPSNdef46762-990a-48b0-b702-15ece1dc541f2
312880salicylic acid 17 % Topical GelPSNdef46762-990a-48b0-b702-15ece1dc541f2
210140salicylic acid 0.17 MG/MG Topical Gel [Compound W brand of salicylic acid]SBDdef46762-990a-48b0-b702-15ece1dc541f2
312880salicylic acid 0.17 MG/MG Topical GelSCDdef46762-990a-48b0-b702-15ece1dc541f2
210140Compound W brand of salicylic acid 0.17 MG/MG Topical GelSYdef46762-990a-48b0-b702-15ece1dc541f2
210140Compound W brand of salicylic acid 17 % Topical GelSYdef46762-990a-48b0-b702-15ece1dc541f2
312880salicylic acid 17 % Topical GelSYdef46762-990a-48b0-b702-15ece1dc541f2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49354-003-00493540003007 g in 1 TUBE7 gHistorical
49354-130-00493540130001 KIT in 1 KIT (49354-130-00) * 1 TUBE in 1 CARTON (49354-003-00) / 7 g in 1 TUBE1 kit2022-12-050000-00-00NoNoCurrent