Salicylic Acid

Product NDC
41520-569
11-digit product format
415200569
Labeler code
41520
Product ID
41520-569_40ab9cf6-ca9f-8520-e063-6394a90a04b2
Type
HUMAN OTC DRUG
Nonproprietary name
Liquid Corn and Callus Remover
Dosage form
LIQUID
Route
TOPICAL
Labeler
Foodhold USA
Application
M030
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-10-20
Substance
SALICYLIC ACID
Active strength
.17 mg/9.8g
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/9.8g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO414PZ4LPZ

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41520-569-03Salicylic Acid9.8 g in 1 PACKAGELIQUID9.811

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41520-569SALICYLIC ACID (LIQUID CORN AND CALLUS REMOVER) LIQUID [FOODHOLD USA]10Current NDC, Legacy NDC, 1 package rows20241109_966889e5-65d9-4057-ac7d-0f985e7c6734.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41520-569-03415200569039.8 g in 1 PACKAGE (41520-569-03) 9.8 g2017-10-200000-00-00NoNoCurrent