Home NDC 71229-102 FUNGINIX ANTI-FUNGAL TREATMENT
Product NDC 71229-102
11-digit product format 712290102
Labeler code 71229
Product ID 71229-102_55a356a6-98f9-aa7a-e063-6294a90ac500
Type HUMAN OTC DRUG
Nonproprietary name UNDECYLENIC ACID
Dosage form OINTMENT
Route TOPICAL
Labeler The Sisquoc Healthcare Corporation
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-03-25
Substance UNDECYLENIC ACID
Active strength 10 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 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 71229-102-11 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 71229-102-11 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 71229-102-11 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 FUNGINIX ANTI-FUNGAL TREATMENT
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength UNDECYLENIC ACID 10 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K3D86KJ24N Internal UNII 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 71229-102-11 FUNGINIX ANTI-FUNGAL TREATMENT 30 mL in 1 TUBE OINTMENT 30 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71229-102 FUNGINIX ANTI-FUNGAL TREATMENT (UNDECYLENIC ACID) OINTMENT [THE SISQUOC HEALTHCARE CORPORATION] 8 Current NDC, Legacy NDC, 1 package rows 20250423_92db5433-5a1b-4cb9-b8eb-217c2a807a99.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71229-102-11 71229010211 30 mL in 1 TUBE (71229-102-11) 30 ml 2019-03-25 0000-00-00 No No Current