FDA.reportPublic FDA data

Tolnaftate

Product NDC
11673-586
11-digit product format
116730586
Labeler code
11673
Product ID
11673-586_c77c61c7-e580-59b0-e053-2995a90a5598
Type
HUMAN OTC DRUG
Nonproprietary name
Antifungal Powder Spray with Baking Soda
Dosage form
AEROSOL, POWDER
Route
TOPICAL
Labeler
Target Corporation
Application
part333C
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2008-12-31
Marketing end
0000-00-00
Substance
TOLNAFTATE
Active strength
1 g/113.3g
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct11673-586DDiscontinued by firm2026-10-05
excluded packagepackage11673-58611673-586-03DDiscontinued by firm2026-10-05

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 · 4 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage11673-586-03d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage11673-586-03f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
11673-586-03GM - Gram11673-586dea4db7a-989b-4e38-9828-ddcd0828981b12013-10-17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TOLNAFTATEACTIVE INGREDIENT06KB629TKVTOLNAFTATE (ANTIFUNGAL POWDER SPRAY WITH BAKING SODA) AEROSOL, POWDER [TARGET CORPORATION]1
TOLNAFTATEACTIVE MOIETY06KB629TKVTOLNAFTATE (ANTIFUNGAL POWDER SPRAY WITH BAKING SODA) AEROSOL, POWDER [TARGET CORPORATION]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MTOLNAFTATE (ANTIFUNGAL POWDER SPRAY WITH BAKING SODA) AEROSOL, POWDER [TARGET CORPORATION]1
DISTEARDIMONIUM HECTORITEINACTIVE INGREDIENTX687XDK09LTOLNAFTATE (ANTIFUNGAL POWDER SPRAY WITH BAKING SODA) AEROSOL, POWDER [TARGET CORPORATION]1
ISOBUTANEINACTIVE INGREDIENTBXR49TP611TOLNAFTATE (ANTIFUNGAL POWDER SPRAY WITH BAKING SODA) AEROSOL, POWDER [TARGET CORPORATION]1
ISOPROPYL MYRISTATEINACTIVE INGREDIENT0RE8K4LNJSTOLNAFTATE (ANTIFUNGAL POWDER SPRAY WITH BAKING SODA) AEROSOL, POWDER [TARGET CORPORATION]1
SODIUM BICARBONATEINACTIVE INGREDIENT8MDF5V39QOTOLNAFTATE (ANTIFUNGAL POWDER SPRAY WITH BAKING SODA) AEROSOL, POWDER [TARGET CORPORATION]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-586TOLNAFTATE (ANTIFUNGAL POWDER SPRAY WITH BAKING SODA) AEROSOL, POWDER [TARGET CORPORATION]11Legacy NDC20241213_522a7247-0e8d-4225-a931-85805238646d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-586-0311673058603113.3 g in 1 CANISTER (11673-586-03) 113.3 g2008-12-310000-00-00NoNoCurrent