Home NDC 29784-181 ProClearz
Product NDC 29784-181
11-digit product format 297840181
Labeler code 29784
Product ID 29784-181_4c0c1702-95ab-d4ad-e063-6294a90afb7c
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate
Dosage form SOLUTION
Route TOPICAL
Labeler Rooftop Consumer Health, Inc.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-10-22
Substance TOLNAFTATE
Active strength 10 mg/mL
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 ProClearz
Brand name suffix Maximum Strength Fungal Shield Brush-on Antifungal
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 06KB629TKV Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 313423 Internal RxNorm lookup 1311221 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 29784-181-01 ProClearzMaximum Strength Fungal Shield Brush-on Antifungal 30 mL in 1 BOTTLE, WITH APPLICATOR SOLUTION 30 38 29784-181-02 ProClearzMaximum Strength Fungal Shield Brush-on Antifungal 1 in 1 BOX SOLUTION 1 38
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 29784-181 PROCLEARZ MAXIMUM STRENGTH FUNGAL SHIELD BRUSH-ON ANTIFUNGAL (TOLNAFTATE) SOLUTION [ROOFTOP CONSUMER HEALTH, INC.] 36 Current NDC, Legacy NDC, 2 package rows 20250105_4d451e87-c25b-49cf-92b8-747b053930c2.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 8 of 49 · 973 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 29784-181-01 29784018101 30 mL in 1 BOTTLE, WITH APPLICATOR 30 ml Historical 29784-181-02 29784018102 1 BOTTLE, WITH APPLICATOR in 1 BOX (29784-181-02) / 30 mL in 1 BOTTLE, WITH APPLICATOR (29784-181-01) 2012-10-22 0000-00-00 No No Current