Tolnaftate

Product NDC
11822-0782
11-digit product format
118220782
Labeler code
11822
Product ID
11822-0782_38107f11-b1bf-fa22-e063-6394a90a2eac
Type
HUMAN OTC DRUG
Nonproprietary name
Jock Itch Powder
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Rite Aid Corporation
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-03-15
Marketing end
2028-03-31
Substance
TOLNAFTATE
Active strength
1.3 g/130g
NDC exclude flag
No
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Tolnaftate

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE1.3 g/130g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui705934

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-0782-42023-01-31C16284748780-1f386c649-dbf9-0266-e053-dadaa90a7c1aRite Aid Antifungal Jock Itch Powder Spray Tolnaftate 1%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-0782-4Tolnaftate130 g in 1 CANAEROSOL, SPRAY1306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-0782TOLNAFTATE (JOCK ITCH POWDER) AEROSOL, SPRAY [RITE AID CORPORATION]5Current NDC, Legacy NDC, 1 package rows20241213_b6968587-45c2-d2f8-e053-2a95a90a8401.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
705934tolnaftate 1 % Powder SprayPSNb6968587-45c2-d2f8-e053-2a95a90a84016
705934tolnaftate 0.01 MG/MG Powder SpraySCDb6968587-45c2-d2f8-e053-2a95a90a84016
705934tolnaftate 1 % Powder SpraySYb6968587-45c2-d2f8-e053-2a95a90a84016

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0782-411822078204130 g in 1 CAN (11822-0782-4) 130 g2021-03-152028-03-31NoNoCurrent