Tolnafate

Product NDC
79481-0607
11-digit product format
794810607
Labeler code
79481
Product ID
79481-0607_4265f839-4aba-acd1-e063-6394a90a8d7f
Type
HUMAN OTC DRUG
Nonproprietary name
Tolnaftate Powder Spray
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Meijer Distribution Inc.
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-08-18
Substance
TOLNAFTATE
Active strength
10 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE10 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui705934

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-0607-1Tolnafate130 g in 1 CANAEROSOL, SPRAY1306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79481-0607TOLNAFATE (TOLNAFTATE POWDER SPRAY) AEROSOL, SPRAY [MEIJER DISTRIBUTION INC.]5Current NDC, 1 package rows20241016_0370c9fa-b986-3a63-e063-6294a90a7627.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
705934tolnaftate 1 % Powder SprayPSN0370c9fa-b986-3a63-e063-6294a90a76276
705934tolnaftate 0.01 MG/MG Powder SpraySCD0370c9fa-b986-3a63-e063-6294a90a76276
705934tolnaftate 1 % Powder SpraySY0370c9fa-b986-3a63-e063-6294a90a76276

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
79481-0607-179481060701130 g in 1 CAN (79481-0607-1) 130 g2023-08-18NoNoHistorical