FDA.reportPublic FDA data

Premier Solutions Liquid Corn and Callus Remover

Product NDC
56104-255
11-digit product format
561040255
Labeler code
56104
Product ID
56104-255_512c81d9-955a-c75f-e063-6294a90a83d4
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic Acid
Dosage form
LIQUID
Route
TOPICAL
Labeler
Premier Brands of America Inc.
Application
M030
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-06-15
Substance
SALICYLIC ACID
Active strength
.17 mg/9.8mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Premier Solutions Liquid Corn and Callus Remover
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID.17 mg/9.8mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO414PZ4LPZ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56104-255-01Premier Solutions Liquid Corn and Callus Remover9.8 mL in 1 PACKAGELIQUID9.86
56104-255-10Premier Solutions Liquid Corn and Callus Remover9.8 mL in 1 BOTTLE, WITH APPLICATORLIQUID9.86
56104-255-10Premier Solutions Liquid Corn and Callus Remover1 in 1 CARTONLIQUID16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56104-255PREMIER SOLUTIONS LIQUID CORN AND CALLUS REMOVER (SALICYLIC ACID) LIQUID [PREMIER BRANDS OF AMERICA INC.]4Current NDC, Legacy NDC, 3 package rows20241016_e16d0256-1151-8394-e053-2995a90ab56c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
56104-255-01561040255019.8 mL in 1 PACKAGE (56104-255-01) 9.8 ml2022-06-150000-00-00NoNoCurrent
56104-255-10561040255101 BOTTLE, WITH APPLICATOR in 1 CARTON (56104-255-10) / 9.8 mL in 1 BOTTLE, WITH APPLICATOR2026-05-08NoNoHistorical