Home NDC 83004-003-01 Migraine Relief
Product NDC 83004-003
Requested package NDC 83004-003-01
11-digit product format 830040003
Labeler code 83004
Product ID 83004-003_2fc154a7-735f-f3fc-e063-6294a90adb82
Type HUMAN OTC DRUG
Nonproprietary name turmeric, curcuma aromatica root, indian frankincense, ginger, feverfew
Dosage form POWDER
Route ORAL
Labeler Rida LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2023-04-15
Substance CURCUMA AROMATICA ROOT; FEVERFEW; GINGER; INDIAN FRANKINCENSE; TURMERIC
Active strength 4; 3; 5; 4; 2 [hp_X]/6g; [hp_X]/6g; [hp_X]/6g; [hp_X]/6g; [hp_X]/6g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
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 · 7 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Migraine Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TURMERIC 4 [hp_X]/6g CURCUMA AROMATICA ROOT 3 [hp_X]/6g INDIAN FRANKINCENSE 5 [hp_X]/6g GINGER 4 [hp_X]/6g FEVERFEW 2 [hp_X]/6g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 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 83004-003-01 Migraine Relief 20 in 1 BOX POWDER 20 2 83004-003-01 Migraine Relief 6 g in 1 PACKET POWDER 6 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83004-003 MIGRAINE RELIEF (TURMERIC, CURCUMA AROMATICA ROOT, INDIAN FRANKINCENSE, GINGER, FEVERFEW) POWDER [RIDA LLC] 2 Current NDC, 2 package rows 20250327_3ac87193-198b-49a6-98b8-e925441d578c.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83004-003-01 83004000301 20 PACKET in 1 BOX (83004-003-01) / 6 g in 1 PACKET 20 packet 2023-04-15 No No Current