Tolnaftate

Product NDC
36800-877
11-digit product format
368000877
Labeler code
36800
Product ID
36800-877_42f46e40-878c-7e09-e063-6294a90ae903
Type
HUMAN OTC DRUG
Nonproprietary name
Tolnaftate Jock Itch Powder Spray Talc Free
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Topco Associates LLC
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-10-31
Substance
TOLNAFTATE
Active strength
1.3 g/130g
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
TOLNAFTATE1.3 g/130g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui705934

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
36800-877-46Tolnaftate130 g in 1 CANAEROSOL, SPRAY1307

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
36800-877TOLNAFTATE (TOLNAFTATE JOCK ITCH POWDER SPRAY TALC FREE) AEROSOL, SPRAY [TOPCO ASSOCIATES LLC]6Current NDC, Legacy NDC, 1 package rows20241213_5f8ac6b7-c46c-226c-e053-2991aa0a9606.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
705934tolnaftate 1 % Powder SprayPSN5f8ac6b7-c46c-226c-e053-2991aa0a96067
705934tolnaftate 0.01 MG/MG Powder SpraySCD5f8ac6b7-c46c-226c-e053-2991aa0a96067
705934tolnaftate 1 % Powder SpraySY5f8ac6b7-c46c-226c-e053-2991aa0a96067

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
36800-877-4636800087746130 g in 1 CAN (36800-877-46) 130 g2017-10-310000-00-00NoNoCurrent