Dakota Muscle Relief

Product NDC
71680-001
11-digit product format
716800001
Labeler code
71680
Product ID
71680-001_7207aaa1-1ea3-41c6-ad58-609063012405
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, UNSPECIFIED FORM
Dosage form
SPRAY
Route
TOPICAL
Labeler
LaShe Naturals, LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2008-07-01
Marketing end
0000-00-00
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
60 mg/mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71680-001-022025-01-30C16284748780-12cef2736-8661-d83d-e063-dadaa90ab31fDakota Muscle Relief
71680-001-082025-01-30C16284748780-12cef2736-8661-d83d-e063-dadaa90ab31fDakota Muscle Relief

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71680-001DAKOTA MUSCLE RELIEF (MENTHOL, UNSPECIFIED FORM) SPRAY [LASHE NATURALS, LLC]3Legacy NDC20211212_160de12b-3f56-40c4-a048-3617567d2ab4.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71680-001-027168000010260 mL in 1 BOTTLE, PLASTIC (71680-001-02) 60 ml2017-09-190000-00-00NoNoCurrent
71680-001-0871680000108240 mL in 1 BOTTLE, PLASTIC (71680-001-08) 240 ml2017-09-190000-00-00NoNoCurrent