FDA.reportPublic FDA data

Salicylic Acid

Product NDC
55315-366
Requested package NDC
55315-366-31
11-digit product format
553150366
Labeler code
55315
Product ID
55315-366_c7914643-f1a4-4581-e053-2995a90acb13
Type
HUMAN OTC DRUG
Nonproprietary name
Corn and Callus Remover Liquid
Dosage form
LIQUID
Route
TOPICAL
Labeler
Fred
Application
part358F
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2015-09-01
Marketing end
0000-00-00
Substance
SALICYLIC ACID
Active strength
0 mg/9.8mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage55315-36655315-366-31DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 8 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZSALICYLIC ACID (CORN AND CALLUS REMOVER LIQUID) LIQUID [FRED’S STORES OF TENNESSEE, INC]1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZSALICYLIC ACID (CORN AND CALLUS REMOVER LIQUID) LIQUID [FRED’S STORES OF TENNESSEE, INC]1
CAMPHOR (NATURAL)INACTIVE INGREDIENTN20HL7Q941SALICYLIC ACID (CORN AND CALLUS REMOVER LIQUID) LIQUID [FRED’S STORES OF TENNESSEE, INC]1
CASTOR OILINACTIVE INGREDIENTD5340Y2I9GSALICYLIC ACID (CORN AND CALLUS REMOVER LIQUID) LIQUID [FRED’S STORES OF TENNESSEE, INC]1
PYROXYLININACTIVE INGREDIENTKYR8BR2X6OSALICYLIC ACID (CORN AND CALLUS REMOVER LIQUID) LIQUID [FRED’S STORES OF TENNESSEE, INC]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55315-366-31553150366319.8 mL in 1 BOTTLE, WITH APPLICATOR (55315-366-31) 9.8 ml2015-09-010000-00-00NoNoCurrent