Home NDC 50367-100 FLUEndz
Product NDC 50367-100
11-digit product format 503670100
Labeler code 50367
Product ID 50367-100_d338e7ef-67ed-461f-ac55-9d9610c275e7
Type HUMAN OTC DRUG
Nonproprietary name Asafoetida, Astragalus Menziesii, Illicium Anisatum, Lonicera Zylosteum
Dosage form SPRAY
Route ORAL
Labeler Herbology International LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2010-01-15
Marketing end 0000-00-00
Substance ASAFETIDA; ASTRAGALUS NUTTALLII LEAF; STAR ANISE; LONICERA XYLOSTEUM FRUIT
Active strength 3 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL
NDC exclude flag E
Listing certified through 2018-12-31
Current FDA listing Historical FDA.report record 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 · 44 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 50367-100-01 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 50367-100-01 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 50367-100-01 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 50367-100-01 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 50367-100-01 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 50367-100-01 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 50367-100-01 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 50367-100-01 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 50367-100-01 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 50367-100-01 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 50367-100-01 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 50367-100-01 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 50367-100-01 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 50367-100-01 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 50367-100-01 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 50367-100-01 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 50367-100-01 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 50367-100-01 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 50367-100-01 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 50367-100-01 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 50367-100-01 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 50367-100-01 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Additional Listing Data#
Finished product Yes
Brand name base FLUEndz Active Ingredients# Ingredient, Strength table Ingredient Strength ASAFETIDA 3 [hp_X]/20mL ASTRAGALUS NUTTALLII LEAF 6 [hp_X]/20mL STAR ANISE 6 [hp_X]/20mL LONICERA XYLOSTEUM FRUIT 1 [hp_X]/20mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 50367-100-01 FLUEndz 20 mL in 1 BOTTLE SPRAY 20 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASAFETIDA ACTIVE INGREDIENT W9FZA51AS1 FLUENDZ (ASAFOETIDA, ASTRAGALUS MENZIESII, ILLICIUM ANISATUM, LONICERA ZYLOSTEUM) SPRAY [HERBOLOGY INTERNATIONAL LLC] 4 ASTRAGALUS NUTTALLII LEAF ACTIVE INGREDIENT NC1P15G4KZ FLUENDZ (ASAFOETIDA, ASTRAGALUS MENZIESII, ILLICIUM ANISATUM, LONICERA ZYLOSTEUM) SPRAY [HERBOLOGY INTERNATIONAL LLC] 4 LONICERA XYLOSTEUM FRUIT ACTIVE INGREDIENT C21POX0M8J FLUENDZ (ASAFOETIDA, ASTRAGALUS MENZIESII, ILLICIUM ANISATUM, LONICERA ZYLOSTEUM) SPRAY [HERBOLOGY INTERNATIONAL LLC] 4 STAR ANISE ACTIVE INGREDIENT XKC1657P78 FLUENDZ (ASAFOETIDA, ASTRAGALUS MENZIESII, ILLICIUM ANISATUM, LONICERA ZYLOSTEUM) SPRAY [HERBOLOGY INTERNATIONAL LLC] 4 ASAFETIDA ACTIVE MOIETY W9FZA51AS1 FLUENDZ (ASAFOETIDA, ASTRAGALUS MENZIESII, ILLICIUM ANISATUM, LONICERA ZYLOSTEUM) SPRAY [HERBOLOGY INTERNATIONAL LLC] 4 ASTRAGALUS NUTTALLII LEAF ACTIVE MOIETY NC1P15G4KZ FLUENDZ (ASAFOETIDA, ASTRAGALUS MENZIESII, ILLICIUM ANISATUM, LONICERA ZYLOSTEUM) SPRAY [HERBOLOGY INTERNATIONAL LLC] 4 LONICERA XYLOSTEUM FRUIT ACTIVE MOIETY C21POX0M8J FLUENDZ (ASAFOETIDA, ASTRAGALUS MENZIESII, ILLICIUM ANISATUM, LONICERA ZYLOSTEUM) SPRAY [HERBOLOGY INTERNATIONAL LLC] 4 STAR ANISE ACTIVE MOIETY XKC1657P78 FLUENDZ (ASAFOETIDA, ASTRAGALUS MENZIESII, ILLICIUM ANISATUM, LONICERA ZYLOSTEUM) SPRAY [HERBOLOGY INTERNATIONAL LLC] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50367-100 FLUENDZ (ASAFOETIDA, ASTRAGALUS MENZIESII, ILLICIUM ANISATUM, LONICERA ZYLOSTEUM) SPRAY [HERBOLOGY INTERNATIONAL LLC] 4 Legacy NDC, 1 package rows 20100208_3ddf6b45-6794-43a6-828d-cc53ae809994.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 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join FLUEndz ASAFOETIDA, ASTRAGALUS MENZIESII, ILLICIUM ANISATUM, LONICERA ZYLOSTEUM Herbology International LLC 3ddf6b45-6794-43a6-828d-cc53ae809994 2026-07-30 Warnings Exact identifier ndc (product): 50367-100
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Status 50367-100-01 50367010001 20 mL in 1 BOTTLE (50367-100-01) 20 ml 2010-01-15 2026-08-31 0 Historical