Home NDC 67234-032 NATUREPLEX TOLNAFTATE
Product NDC 67234-032
11-digit product format 672340032
Labeler code 67234
Product ID 67234-032_32b1b1ae-2200-479a-bc9e-a203595ef6d3
Type HUMAN OTC DRUG
Nonproprietary name TOLNAFTATE
Dosage form CREAM
Route TOPICAL
Labeler Natureplex, LLC
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 1993-09-23
Substance TOLNAFTATE
Active strength 10 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 67234-032 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 67234-032 67234-032-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 NATUREPLEX TOLNAFTATE
Brand name suffix ANTIFUNGAL
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE 10 mg/g
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 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 103951 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 67234-032-01 NATUREPLEX TOLNAFTATE ANTIFUNGAL 1 in 1 CARTON CREAM 1 3 67234-032-01 NATUREPLEX TOLNAFTATE ANTIFUNGAL 28 g in 1 TUBE CREAM 28 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67234-032 NATUREPLEX TOLNAFTATE ANTIFUNGAL (TOLNAFTATE) CREAM [NATUREPLEX, LLC] 3 Current NDC, Legacy NDC, 2 package rows 20250119_575b8645-9166-4242-a74f-f4aa4acaaf3d.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 51 · 1,004 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 67234-032-01 67234003201 1 TUBE in 1 CARTON (67234-032-01) / 28 g in 1 TUBE 1 tube 1993-09-23 0000-00-00 No No Current