Home NDC 57520-0424 Restless Legs Relief
Product NDC 57520-0424
11-digit product format 575200424
Labeler code 57520
Product ID 57520-0424_a434d123-4144-40a0-8914-0cdbf3eeea31
Type HUMAN OTC DRUG
Nonproprietary name Gnaphalium polycephalum, Viscum album, Aconitum napellus, Ledum palustre, Magnesia phosphorica, Rhus toxicodendron,
Dosage form TABLET
Route ORAL
Labeler Apotheca Company
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2010-11-16
Marketing end 0000-00-00
Substance PSEUDOGNAPHALIUM OBTUSIFOLIUM; VISCUM ALBUM FRUITING TOP; ACONITUM NAPELLUS; LEDUM PALUSTRE TWIG; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; TOXICODENDRON PUBESCENS LEAF
Active strength 4 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 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 57520-0424-1 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57520-0424-1 Restless Legs Relief 125 in 1 BOTTLE TABLET 125 2
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACONITUM NAPELLUS ACTIVE INGREDIENT U0NQ8555JD RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 LEDUM PALUSTRE TWIG ACTIVE INGREDIENT 877L01IZ0P RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE ACTIVE INGREDIENT HF539G9L3Q RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 PSEUDOGNAPHALIUM OBTUSIFOLIUM ACTIVE INGREDIENT 36XQ854NWW RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 TOXICODENDRON PUBESCENS LEAF ACTIVE INGREDIENT 6IO182RP7A RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 VISCUM ALBUM FRUITING TOP ACTIVE INGREDIENT BK9092J5MP RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 ACONITUM NAPELLUS ACTIVE MOIETY U0NQ8555JD RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 LEDUM PALUSTRE TWIG ACTIVE MOIETY 877L01IZ0P RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 MAGNESIUM CATION ACTIVE MOIETY T6V3LHY838 RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 PSEUDOGNAPHALIUM OBTUSIFOLIUM ACTIVE MOIETY 36XQ854NWW RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 TOXICODENDRON PUBESCENS LEAF ACTIVE MOIETY 6IO182RP7A RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 VISCUM ALBUM FRUITING TOP ACTIVE MOIETY BK9092J5MP RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 LACTOSE INACTIVE INGREDIENT J2B2A4N98G RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57520-0424 RESTLESS LEGS RELIEF (GNAPHALIUM POLYCEPHALUM, VISCUM ALBUM, ACONITUM NAPELLUS, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOXICODENDRON,) TABLET [APOTHECA COMPANY] 2 Legacy NDC, 1 package rows 20110517_256fba47-1a4d-475f-84be-a6b36d63a096.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 57520-0424-1 57520042401 125 in 1 BOTTLE Historical