PHYTOZINE RINGWORM TREATMENT

Product NDC
71229-101
11-digit product format
712290101
Labeler code
71229
Product ID
71229-101_334f4f69-fe0c-c703-e063-6394a90adecf
Type
HUMAN OTC DRUG
Nonproprietary name
TOLNAFTATE
Dosage form
OINTMENT
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
PHYTOZINE RINGWORM TREATMENT
Brand name suffix
MAXIMUM STRENGTH
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE1 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui199126

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71229-101-11PHYTOZINE RINGWORM TREATMENTMAXIMUM STRENGTH28 g in 1 TUBEOINTMENT286

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71229-101PHYTOZINE RINGWORM TREATMENT MAXIMUM STRENGTH (TOLNAFTATE) OINTMENT [THE SISQUOC HEALTHCARE CORPORATION]6Current NDC, Legacy NDC, 1 package rows20250423_5dff6ee7-f7a9-4841-8357-6b0801d253f1.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199126tolnaftate 1 % Topical OintmentPSN5dff6ee7-f7a9-4841-8357-6b0801d253f16
199126tolnaftate 0.01 MG/MG Topical OintmentSCD5dff6ee7-f7a9-4841-8357-6b0801d253f16
199126tolnaftate 1 % Topical OintmentSY5dff6ee7-f7a9-4841-8357-6b0801d253f16

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71229-101-117122901011128 g in 1 TUBE (71229-101-11) 28 g2019-03-250000-00-00NoNoCurrent