Meijer Maximum Strength Jock Itch Relief Antifungal

Product NDC
23667-809
11-digit product format
236670809
Labeler code
23667
Product ID
23667-809_0b82602d-37c1-0320-e063-6394a90a724c
Type
HUMAN OTC DRUG
Nonproprietary name
TOLNAFTATE
Dosage form
SPRAY
Route
TOPICAL
Labeler
Formulated Solutions, LLC
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-01-21
Substance
TOLNAFTATE
Active strength
10 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Meijer Maximum Strength Jock Itch Relief Antifungal
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE10 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui705934

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23667-809-01Meijer Maximum Strength Jock Itch Relief Antifungal130 g in 1 CANSPRAY1302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23667-809MEIJER MAXIMUM STRENGTH JOCK ITCH RELIEF ANTIFUNGAL (TOLNAFTATE) SPRAY [FORMULATED SOLUTIONS, LLC]2Current NDC, Legacy NDC, 1 package rows20231207_46c5b9a6-99ea-7343-e054-00144ff88e88.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
705934tolnaftate 1 % Powder SprayPSN46c5b9a6-99ea-7343-e054-00144ff88e882
705934tolnaftate 0.01 MG/MG Powder SpraySCD46c5b9a6-99ea-7343-e054-00144ff88e882
705934tolnaftate 1 % Powder SpraySY46c5b9a6-99ea-7343-e054-00144ff88e882

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
23667-809-0123667080901130 g in 1 CAN (23667-809-01) 130 g2017-01-210000-00-00NoNoCurrent