Home NDC 70000-0322 Tolnafate
Product NDC 70000-0322
11-digit product format 700000322
Labeler code 70000
Product ID 70000-0322_5d435356-1461-d622-e063-6294a90ad90d
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate Powder Spray - Talc Free
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler LEADER/ Cardinal Health 110, Inc.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-10-20
Substance TOLNAFTATE
Active strength 1.3 g/130g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Tolnafate
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE 1.3 g/130g
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70000-0322-1 Tolnafate 130 g in 1 CAN AEROSOL, SPRAY 130 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70000-0322 TOLNAFATE (TOLNAFTATE POWDER SPRAY - TALC FREE) AEROSOL, SPRAY [LEADER/ CARDINAL HEALTH 110, INC.] 8 Current NDC, Legacy NDC, 1 package rows 20241103_a9fdd129-9909-4747-bd9f-93a204b50724.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 36 of 49 · 969 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70000-0322-1 70000032201 130 g in 1 CAN (70000-0322-1) 130 g 2017-10-20 0000-00-00 No No Current