Home NDC 71171-778 ELON Dual Defense Anti Fungal Formula
Product NDC 71171-778
11-digit product format 711710778
Labeler code 71171
Product ID 71171-778_2cc52b1d-28d2-6315-e063-6294a90a46c0
Type HUMAN OTC DRUG
Nonproprietary name UNDECYLENIC ACID
Dosage form LIQUID
Route TOPICAL
Labeler Little Giant Holdings LLC
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-01-02
Substance UNDECYLENIC ACID
Active strength 250 mg/mL
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 · 4 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 2025-01-20 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 71171-778-15 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 71171-778-15 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 ELON Dual Defense Anti Fungal Formula
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength UNDECYLENIC ACID 250 mg/mL
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 998329 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 71171-778-15 ELON Dual Defense Anti Fungal Formula 15 mL in 1 BOTTLE LIQUID 15 3 71171-778-15 ELON Dual Defense Anti Fungal Formula 1 in 1 BOX LIQUID 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71171-778 ELON DUAL DEFENSE ANTI FUNGAL FORMULA (UNDECYLENIC ACID) LIQUID [LITTLE GIANT HOLDINGS LLC] 3 Current NDC, Legacy NDC, 2 package rows 20250130_45c4567d-7876-6459-e054-00144ff88e88.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 71171-778-15 71171077815 1 BOTTLE in 1 BOX (71171-778-15) / 15 mL in 1 BOTTLE 1 bottle 2017-01-02 0000-00-00 No No Current