Salicylic Acid

Product NDC
41520-567
11-digit product format
415200567
Labeler code
41520
Product ID
41520-567_422aa9d5-f08a-2b69-e063-6294a90a4b97
Type
HUMAN OTC DRUG
Nonproprietary name
Wart Remover Gel
Dosage form
GEL
Route
TOPICAL
Labeler
Foodhold USA
Application
M028
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-10-20
Substance
SALICYLIC ACID
Active strength
.17 g/7g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Salicylic Acid
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID.17 g/7g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO414PZ4LPZ

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41520-567-25Salicylic Acid7 g in 1 TUBEGEL79

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41520-567SALICYLIC ACID (WART REMOVER GEL) GEL [FOODHOLD USA]8Current NDC, Legacy NDC, 1 package rows20241109_fbcf110c-a891-4207-aeb8-a878baf223e0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41520-567-25415200567257 g in 1 TUBE (41520-567-25) 7 g2017-10-200000-00-00NoNoCurrent