Derman Antifungal

Product NDC
54312-230
11-digit product format
543120230
Labeler code
54312
Product ID
54312-230_4c4d682d-dea0-cfe0-e063-6394a90a741e
Type
HUMAN OTC DRUG
Nonproprietary name
TOLNAFTATE
Dosage form
AEROSOL, POWDER
Route
TOPICAL
Labeler
Compania Internacional de Comercio, S.A.P.I. de C.V.
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-11-13
Substance
TOLNAFTATE
Active strength
10 mg/g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE10 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui705934

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54312-230-01Derman Antifungal130 g in 1 BOTTLE, SPRAYAEROSOL, POWDER1303

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
705934tolnaftate 1 % Powder SprayPSN5784a783-1056-4d50-8d87-2df4f8e16b093
705934tolnaftate 0.01 MG/MG Powder SpraySCD5784a783-1056-4d50-8d87-2df4f8e16b093
705934tolnaftate 1 % Powder SpraySY5784a783-1056-4d50-8d87-2df4f8e16b093

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
54312-230-0154312023001130 g in 1 BOTTLE, SPRAY (54312-230-01) 130 g2025-11-13NoNoCurrent