Fungicure Anti-Fungal Liquid

Product NDC
52389-298
11-digit product format
523890298
Labeler code
52389
Product ID
52389-298_4e67ab01-b191-35e8-e063-6294a90a51df
Type
HUMAN OTC DRUG
Nonproprietary name
Tolnaftate
Dosage form
LIQUID
Route
TOPICAL
Labeler
Kobayashi Healthcare International, Inc.
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-10-13
Substance
TOLNAFTATE
Active strength
8.65 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Fungicure Anti-Fungal Liquid
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE8.65 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52389-298-30Fungicure Anti-Fungal Liquid30 mL in 1 BOTTLE, WITH APPLICATORLIQUID309
52389-298-30Fungicure Anti-Fungal Liquid1 in 1 BOXLIQUID19
52389-298-40Fungicure Anti-Fungal Liquid40 mL in 1 BOTTLE, WITH APPLICATORLIQUID409
52389-298-40Fungicure Anti-Fungal Liquid1 in 1 BOXLIQUID19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52389-298FUNGICURE ANTI-FUNGAL LIQUID (TOLNAFTATE) LIQUID [KOBAYASHI HEALTHCARE INTERNATIONAL, INC.]6Current NDC, Legacy NDC, 4 package rows20250412_b18ee199-0659-733c-e053-2a95a90ab6b5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
52389-298-30523890298301 BOTTLE, WITH APPLICATOR in 1 BOX (52389-298-30) / 30 mL in 1 BOTTLE, WITH APPLICATOR2020-10-130000-00-00NoNoCurrent
52389-298-40523890298401 BOTTLE, WITH APPLICATOR in 1 BOX (52389-298-40) > 40 mL in 1 BOTTLE, WITH APPLICATOR2021-04-050000-00-00NoNoCurrent