Salicylic Acid

Product NDC
11822-0120
11-digit product format
118220120
Labeler code
11822
Product ID
11822-0120_3810127d-0137-05b6-e063-6294a90a44f8
Type
HUMAN OTC DRUG
Nonproprietary name
Corn and Callus Remover Liquid
Dosage form
LIQUID
Route
TOPICAL
Labeler
Rite Aid Corporation
Application
M030
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-12-22
Marketing end
2026-06-30
Substance
SALICYLIC ACID
Active strength
.17 mg/9.8mL
NDC exclude flag
No
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Salicylic Acid

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
11822-0120-9Salicylic Acid9.8 mL in 1 BOTTLE, WITH APPLICATORLIQUID9.810

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-0120SALICYLIC ACID (CORN AND CALLUS REMOVER LIQUID) LIQUID [RITE AID CORPORATION]9Current NDC, Legacy NDC, 1 package rows20241213_ea071f97-c4ba-4283-b372-9f4292ad9b2c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0120-9118220120099.8 mL in 1 BOTTLE, WITH APPLICATOR (11822-0120-9) 9.8 ml2017-12-222026-06-30NoNoCurrent