Rugby Antifungal

Product NDC
0536-1481
11-digit product format
005361481
Labeler code
0536
Product ID
0536-1481_51cdb16c-1b3f-d150-e063-6394a90a2d6f
Type
HUMAN OTC DRUG
Nonproprietary name
tolnaftate aerosol, powder
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Rugby Laboratories
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-05-01
Substance
TOLNAFTATE
Active strength
10 mg/g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Rugby Antifungal
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE10 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii06KB629TKV
Rxcui313421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0536-1481-01Rugby Antifungal130 g in 1 CANAEROSOL, SPRAY1302

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
313421tolnaftate 1 % Topical SprayPSN50c46cf5-3e64-9e0f-e063-6294a90a23172
313421tolnaftate 10 MG/ML Topical SpraySCD50c46cf5-3e64-9e0f-e063-6294a90a23172
313421tolnaftate 1 % Topical SpraySY50c46cf5-3e64-9e0f-e063-6294a90a23172

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0536-1481-0100536148101130 g in 1 CAN (0536-1481-01) 130 g2026-05-01NoNoHistorical