Tolnafate

Product NDC
79903-016
11-digit product format
799030016
Labeler code
79903
Product ID
79903-016_5013f5d5-6e21-c298-e063-6294a90ac71c
Type
HUMAN OTC DRUG
Nonproprietary name
Tolnaftate Powder Spray
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Wal-Mart Stores, Inc
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-03-01
Substance
TOLNAFTATE
Active strength
1.3 g/130g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Tolnafate
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE1.3 g/130g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui705934

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-016-46Tolnafate130 g in 1 CANAEROSOL, SPRAY1309

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79903-016TOLNAFATE (TOLNAFTATE POWDER SPRAY) AEROSOL, SPRAY [WAL-MART STORES, INC]5Current NDC, Legacy NDC, 1 package rows20241218_af4dd045-ca51-42b9-e053-2a95a90a0327.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
705934tolnaftate 1 % Powder SprayPSNaf4dd045-ca51-42b9-e053-2a95a90a03279
705934tolnaftate 0.01 MG/MG Powder SpraySCDaf4dd045-ca51-42b9-e053-2a95a90a03279
705934tolnaftate 1 % Powder SpraySYaf4dd045-ca51-42b9-e053-2a95a90a03279

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79903-016-4679903001646130 g in 1 CAN (79903-016-46) 130 g2021-03-010000-00-00NoNoCurrent