Tolnaftate

Product NDC
68016-586
11-digit product format
680160586
Labeler code
68016
Product ID
68016-586_c78dc02d-2973-455f-e053-2a95a90a4a8d
Type
HUMAN OTC DRUG
Nonproprietary name
Foot Odor Control Powder Spray
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Chain Drug Consortium, LLC
Application
part333C
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2006-06-01
Marketing end
0000-00-00
Substance
TOLNAFTATE
Active strength
1 g/113g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68016-586-032023-01-31C16284748780-1f386c649-b85f-0266-e053-dadaa90a7c1a059f540a-3233-435e-b54c-98b2302306e2
68016-586-032023-01-30C16284748780-1f386c649-b85f-0266-e053-dadaa90a7c1a059f540a-3233-435e-b54c-98b2302306e2

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68016-586-03GM - Gram68016-586aff9c028-260c-4fe1-af12-b7ab781d200312022-06-06

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68016-586TOLNAFTATE (FOOT ODOR CONTROL POWDER SPRAY) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC]8Legacy NDC20241213_059f540a-3233-435e-b54c-98b2302306e2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68016-586-0368016058603113 g in 1 CAN (68016-586-03) 113 g2006-06-010000-00-00NoNoCurrent