Fungi Nail Everyday Antifungal Powder

Product NDC
55505-234
11-digit product format
555050234
Labeler code
55505
Product ID
55505-234_70d099e0-4310-47de-9a74-4955ec7305fb
Type
HUMAN OTC DRUG
Nonproprietary name
Tolnaftate
Dosage form
SPRAY
Route
TOPICAL
Labeler
Kramer Laboratories
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-01-01
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
Fungi Nail Everyday Antifungal Powder
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
55505-234-81Fungi Nail Everyday Antifungal Powder130 g in 1 CANSPRAY1301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55505-234FUNGI NAIL EVERYDAY ANTIFUNGAL POWDER (TOLNAFTATE) SPRAY [KRAMER LABORATORIES]1Current NDC, 1 package rows20250101_8ed1a08a-3019-4564-968f-154e659c05e1.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
705934tolnaftate 1 % Powder SprayPSN8ed1a08a-3019-4564-968f-154e659c05e11
705934tolnaftate 0.01 MG/MG Powder SpraySCD8ed1a08a-3019-4564-968f-154e659c05e11
705934tolnaftate 1 % Powder SpraySY8ed1a08a-3019-4564-968f-154e659c05e11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
55505-234-8155505023481130 g in 1 CAN (55505-234-81) 130 g2025-01-01NoNoHistorical