Liquid Wart Remover

Product NDC
56104-245
11-digit product format
561040245
Labeler code
56104
Product ID
56104-245_4097a58b-0d97-59ff-e063-6294a90a0252
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic Acid
Dosage form
LIQUID
Route
TOPICAL
Labeler
Premier Brands of America, Inc.
Application
M028
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-06-16
Substance
SALICYLIC ACID
Active strength
.17 g/9mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Liquid Wart Remover
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID.17 g/9mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO414PZ4LPZ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56104-245-01Liquid Wart Remover9 mL in 1 BOTTLE, WITH APPLICATORLIQUID95

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56104-245LIQUID WART REMOVER (SALICYLIC ACID) LIQUID [PREMIER BRANDS OF AMERICA, INC.]4Current NDC, Legacy NDC, 1 package rows20241013_e1964b8a-b5f1-32a6-e053-2a95a90a6e41.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
56104-245-01561040245019 mL in 1 BOTTLE, WITH APPLICATOR (56104-245-01) 9 ml2022-06-160000-00-00NoNoCurrent