FDA.reportPublic FDA data

ARTHRIT-EASE

Product NDC
71136-770
Requested package NDC
71136-770-04
11-digit product format
711360770
Labeler code
71136
Product ID
71136-770_43b66656-f126-0288-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
CREAM
Route
TOPICAL
Labeler
Atlantic Horizon International Inc.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2016-12-15
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
50 mg/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage71136-77071136-770-04DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71136-770-0471136077004113 g in 1 JAR (71136-770-04) 113 g2016-12-150000-00-00NoNoCurrent