FDA.reportPublic FDA data

Tolnaftate

Product NDC
68016-586
Requested package NDC
68016-586-03
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

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 packagepackage68016-58668016-586-03DDiscontinued by firm2026-09-14

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 packagepackage68016-58668016-586-03DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage68016-58668016-586-03DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68016-586-032023-01-31C16284748780-1f386c649-b85f-0266-e053-dadaa90a7c1aFoot Odor Control Powder Spray
68016-586-032023-01-30C16284748780-1f386c649-b85f-0266-e053-dadaa90a7c1aFoot Odor Control Powder Spray

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#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TOLNAFTATEACTIVE INGREDIENT06KB629TKVTOLNAFTATE (FOOT ODOR CONTROL POWDER SPRAY) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC]2
TOLNAFTATEACTIVE MOIETY06KB629TKVTOLNAFTATE (FOOT ODOR CONTROL POWDER SPRAY) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC]2
ALCOHOLINACTIVE INGREDIENT3K9958V90MTOLNAFTATE (FOOT ODOR CONTROL POWDER SPRAY) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC]2
DISTEARDIMONIUM HECTORITEINACTIVE INGREDIENTX687XDK09LTOLNAFTATE (FOOT ODOR CONTROL POWDER SPRAY) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC]2
ISOBUTANEINACTIVE INGREDIENTBXR49TP611TOLNAFTATE (FOOT ODOR CONTROL POWDER SPRAY) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC]2
ISOPROPYL MYRISTATEINACTIVE INGREDIENT0RE8K4LNJSTOLNAFTATE (FOOT ODOR CONTROL POWDER SPRAY) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC]2
SODIUM BICARBONATEINACTIVE INGREDIENT8MDF5V39QOTOLNAFTATE (FOOT ODOR CONTROL POWDER SPRAY) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC]2

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