FDA.reportPublic FDA data

Cherry Cough Drop

Product NDC
11822-0031
Requested package NDC
11822-0031-1
11-digit product format
118220031
Labeler code
11822
Product ID
11822-0031_ed740383-f676-1870-e053-2995a90a13fa
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
LOZENGE
Route
ORAL
Labeler
Rite Aid
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2013-05-01
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
6 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
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 packagepackage11822-003111822-0031-1DDiscontinued by firm2026-10-05

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
11822-0031CHERRY COUGH DROP (MENTHOL) LOZENGE [RITE AID]7Legacy NDC20241201_4aa03876-8a12-55f6-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0031-11182200310130 LOZENGE in 1 BAG (11822-0031-1) 30 lozenge2013-05-010000-00-00NoNoCurrent