HC Max Anti-Fungal

Product NDC
55505-195
11-digit product format
555050195
Labeler code
55505
Product ID
55505-195_afee6fc1-048c-440c-974f-f6934c7e2934
Type
HUMAN OTC DRUG
Nonproprietary name
Tolnaftate
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Kramer Laboratories
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-05-28
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
HC Max Anti-Fungal
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
55505-195-62HC Max Anti-Fungal150 g in 1 CANAEROSOL, SPRAY1506

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55505-195HC MAX ANTI-FUNGAL (TOLNAFTATE) AEROSOL, SPRAY [KRAMER LABORATORIES]4Current NDC, Legacy NDC, 1 package rows20250101_ee99cd87-549f-4a43-878e-b4d5935de0e0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
313421tolnaftate 1 % Topical SprayPSNee99cd87-549f-4a43-878e-b4d5935de0e06
313421tolnaftate 10 MG/ML Topical SpraySCDee99cd87-549f-4a43-878e-b4d5935de0e06
313421tolnaftate 1 % Topical SpraySYee99cd87-549f-4a43-878e-b4d5935de0e06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55505-195-6255505019562150 g in 1 CAN (55505-195-62) 150 g2020-05-280000-00-00NoNoCurrent