Maximum Strength Antifungal Liquid

Product NDC
0363-2026
11-digit product format
003632026
Labeler code
0363
Product ID
0363-2026_411165dc-10a0-eef6-e063-6394a90a0800
Type
HUMAN OTC DRUG
Nonproprietary name
Tolnaftate
Dosage form
LIQUID
Route
TOPICAL
Labeler
Walgreens Company
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-06-07
Substance
TOLNAFTATE
Active strength
10 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Maximum Strength Antifungal Liquid
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE10 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui313423

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-2026-01Maximum Strength Antifungal Liquid1 in 1 CARTONLIQUID12
0363-2026-01Maximum Strength Antifungal Liquid30 mL in 1 BOTTLE, WITH APPLICATORLIQUID302

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
313423tolnaftate 1 % Topical SolutionPSN3858402f-783b-9292-e063-6294a90abe382
313423tolnaftate 10 MG/ML Topical SolutionSCD3858402f-783b-9292-e063-6294a90abe382
313423tolnaftate 1 % Topical SolutionSY3858402f-783b-9292-e063-6294a90abe382

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
0363-2026-01003632026011 BOTTLE, WITH APPLICATOR in 1 CARTON (0363-2026-01) / 30 mL in 1 BOTTLE, WITH APPLICATOR2024-06-07NoNoCurrent