Lurosil

Product NDC
58697-539
11-digit product format
586970539
Labeler code
58697
Product ID
58697-539_e4dcd54d-6561-47c7-ba02-b1fb494fdbd9
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Pacific Health Collabroative
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2013-06-17
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
3 g/100g
NDC exclude flag
E
Listing certified through
2017-12-31
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
58697-539-022019-11-27C16284748780-19855d018-e32a-cd31-e053-dbdaa90ab51aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58697-539-02Lurosil1 in 1 BOXGEL13
58697-539-02Lurosil57 g in 1 TUBEGEL573

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58697-539LUROSIL (MENTHOL) GEL [PACIFIC HEALTH COLLABROATIVE]3Legacy NDC, 2 package rows20130806_2006567f-4e41-487b-81d7-77b52b51fc4c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
282805menthol 2.5 % Topical GelPSN2006567f-4e41-487b-81d7-77b52b51fc4c3
282805menthol 0.025 MG/MG Topical GelSCD2006567f-4e41-487b-81d7-77b52b51fc4c3
282805menthol 2.5 % Topical GelSY2006567f-4e41-487b-81d7-77b52b51fc4c3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
58697-539-02586970539021 in 1 BOXHistorical