Home NDC 84614-002 TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid
Product NDC 84614-002
11-digit product format 846140002
Labeler code 84614
Product ID 84614-002_48b9ae23-4075-7b2c-e063-6294a90a27e6
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate
Dosage form LIQUID
Route TOPICAL
Labeler Shenzhen Ctrip Technology Co., Ltd.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-08-23
Substance TOLNAFTATE
Active strength 1 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 2025-08-27 00:01 UTC · source 2025-08-26 excluded product product 84614-002 I Inactivated by FDA excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 84614-002 84614-002-01 I Inactivated by FDA excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE 1 g/100mL
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 313423 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84614-002-01 TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid 2 in 1 PACKAGE LIQUID 2 2 84614-002-01 TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid 30 mL in 1 BOTTLE LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84614-002 TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH LIQUID (TOLNAFTATE) LIQUID [SHENZHEN CTRIP TECHNOLOGY CO., LTD.] 1 Current NDC, 2 package rows 20240824_1fb03184-5f21-c82a-e063-6294a90a9fa4.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 Sample Exclude flag Status 84614-002-01 84614000201 2 BOTTLE in 1 PACKAGE (84614-002-01) / 30 mL in 1 BOTTLE 2 bottle 2024-08-23 No No Current