NUTURNA Arthritis Intensive Concentrate for Pain Relief and Recovery

Product NDC
81996-244
Requested package NDC
81996-244-04
11-digit product format
819960244
Labeler code
81996
Product ID
81996-244_c4b6f1b2-c4a5-77a9-e053-2995a90a356d
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
CREAM
Route
TOPICAL
Labeler
Nuturna International LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-11-22
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
4 g/100g
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 packagepackage81996-24481996-244-04DDiscontinued by firm2026-10-15

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage81996-24481996-244-04IInactivated by FDAexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage81996-24481996-244-04IInactivated by FDAexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81996-244-02NUTURNA Arthritis Intensive Concentrate for Pain Relief and Recovery57 g in 1 JARCREAM576
81996-244-04NUTURNA Arthritis Intensive Concentrate for Pain Relief and Recovery114 g in 1 JARCREAM1146
81996-244-08NUTURNA Arthritis Intensive Concentrate for Pain Relief and Recovery228 g in 1 JARCREAM2286

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81996-244NUTURNA ARTHRITIS INTENSIVE CONCENTRATE FOR PAIN RELIEF AND RECOVERY (MENTHOL) CREAM [NUTURNA INTERNATIONAL LLC]6Legacy NDC, 3 package rows20240105_46384348-d48c-485c-aaf0-75a0a688ca85.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1655936menthol 3.7 % Topical CreamPSN46384348-d48c-485c-aaf0-75a0a688ca856
1655936menthol 37 MG/ML Topical CreamSCD46384348-d48c-485c-aaf0-75a0a688ca856
1655936menthol 3.7 % Topical CreamSY46384348-d48c-485c-aaf0-75a0a688ca856

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
81996-244-0481996024404114 g in 1 JAR (81996-244-04) 114 g2021-05-280000-00-00NoNoCurrent