Tolnaftate

Product NDC
21130-213
11-digit product format
211300213
Labeler code
21130
Product ID
21130-213_41eeb7c0-0631-f613-e063-6394a90ab838
Type
HUMAN OTC DRUG
Nonproprietary name
Antifungal Liquid Spray
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Better Living Brands LLC
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-09-27
Substance
TOLNAFTATE
Active strength
1.5 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
TOLNAFTATE1.5 g/150g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui313421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21130-213-00Tolnaftate150 g in 1 CANISTERAEROSOL, SPRAY1505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21130-213TOLNAFTATE (ANTIFUNGAL LIQUID SPRAY) AEROSOL, SPRAY [BETTER LIVING BRANDS LLC]4Current NDC, Legacy NDC, 1 package rows20241109_ccff4830-6d81-2a0d-e053-2a95a90a154c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
313421tolnaftate 1 % Topical SprayPSNccff4830-6d81-2a0d-e053-2a95a90a154c5
313421tolnaftate 10 MG/ML Topical SpraySCDccff4830-6d81-2a0d-e053-2a95a90a154c5
313421tolnaftate 1 % Topical SpraySYccff4830-6d81-2a0d-e053-2a95a90a154c5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21130-213-0021130021300150 g in 1 CANISTER (21130-213-00) 150 g2021-09-270000-00-00NoNoCurrent