FUNGINIX JOCK ITCH TREATMENT

Product NDC
71229-104
11-digit product format
712290104
Labeler code
71229
Product ID
71229-104_2f0087ac-d89a-ebe7-e063-6294a90ad9e8
Type
HUMAN OTC DRUG
Nonproprietary name
TOLNAFTATE
Dosage form
CREAM
Route
TOPICAL
Labeler
The Sisquoc Healthcare Corporation
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-03-25
Substance
TOLNAFTATE
Active strength
1 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
FUNGINIX JOCK ITCH TREATMENT
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE1 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui103951

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71229-104-11FUNGINIX JOCK ITCH TREATMENT28 g in 1 TUBECREAM286

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71229-104FUNGINIX JOCK ITCH TREATMENT (TOLNAFTATE) CREAM [THE SISQUOC HEALTHCARE CORPORATION]6Current NDC, Legacy NDC, 1 package rows20250227_b2ce1c25-93d5-441f-9b3b-68ae46400c2c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
103951tolnaftate 1 % Topical CreamPSNb2ce1c25-93d5-441f-9b3b-68ae46400c2c6
103951tolnaftate 10 MG/ML Topical CreamSCDb2ce1c25-93d5-441f-9b3b-68ae46400c2c6
103951tolnaftate 1 % Topical CreamSYb2ce1c25-93d5-441f-9b3b-68ae46400c2c6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71229-104-117122901041128 g in 1 TUBE (71229-104-11) 28 g2019-03-250000-00-00NoNoCurrent