Salicylic Acid

Product NDC
72446-006
11-digit product format
724460006
Labeler code
72446
Product ID
72446-006_409719f1-18fb-a025-e063-6394a90ad715
Type
HUMAN OTC DRUG
Nonproprietary name
Liquid Wart Remover
Dosage form
LIQUID
Route
TOPICAL
Labeler
Hudson Health LLC
Application
M028
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2018-09-01
Substance
SALICYLIC ACID
Active strength
.17 mg/9mL
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 mg/9mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO414PZ4LPZ

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72446-006-09Salicylic Acid9 mL in 1 BOTTLE, WITH APPLICATORLIQUID98

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72446-006SALICYLIC ACID (LIQUID WART REMOVER) LIQUID [HUDSON HEALTH LLC]7Current NDC, Legacy NDC, 1 package rows20241017_63b62a7a-1082-4323-bf44-810545792de9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72446-006-09724460006099 mL in 1 BOTTLE, WITH APPLICATOR (72446-006-09) 9 ml2018-09-010000-00-00NoNoCurrent