Tolnaftate

Product NDC
30142-147
11-digit product format
301420147
Labeler code
30142
Product ID
30142-147_426530f1-e70d-c6f5-e063-6394a90a05ad
Type
HUMAN OTC DRUG
Nonproprietary name
Antifungal Spray Liquid
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Kroger Co.
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-12-06
Substance
TOLNAFTATE
Active strength
150 g/150g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Tolnaftate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE150 g/150g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30142-147-53Tolnaftate150 g in 1 CANAEROSOL, SPRAY1506

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-147TOLNAFTATE (ANTIFUNGAL SPRAY LIQUID) AEROSOL, SPRAY [KROGER CO.]5Current NDC, Legacy NDC, 1 package rows20241116_0cfebac3-684d-4599-b75f-9a82708db717.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-147-5330142014753150 g in 1 CAN (30142-147-53) 150 g2017-12-060000-00-00NoNoCurrent