FDA.reportPublic FDA data

Salicylic Acid

Product NDC
11822-0121
11-digit product format
118220121
Labeler code
11822
Product ID
11822-0121_c792c72d-4d03-4ec6-e053-2995a90a149a
Type
HUMAN OTC DRUG
Nonproprietary name
Wart Remover Gel
Dosage form
GEL
Route
TOPICAL
Labeler
Rite Aid Corporation
Application
part358B
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2014-10-07
Marketing end
0000-00-00
Substance
SALICYLIC ACID
Active strength
0 g/7g
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct11822-0121DDiscontinued by firm2026-10-15
excluded packagepackage11822-012111822-0121-7DDiscontinued by firm2026-10-15

Reported adverse events (FAERS/openFDA)#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-0121SALICYLIC ACID (WART REMOVER GEL) GEL [RITE AID CORPORATION]7Legacy NDC20241213_725e7cc4-29b9-438e-a260-d93859d78fb1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0121-7118220121077 g in 1 TUBE (11822-0121-7) 7 g2014-10-070000-00-00NoNoCurrent