Home NDC 57520-0272 Fibro Relief
Product NDC 57520-0272
11-digit product format 575200272
Labeler code 57520
Product ID 57520-0272_e1b840f7-a357-448e-bef7-d4ed2b3a43c4
Type HUMAN OTC DRUG
Nonproprietary name Ferrum metallicum, Guaiacum, Lithium carbonicum, Lycopersicum esculentum, Magnesia phosphorica
Dosage form CAPSULE
Route ORAL
Labeler Apotheca Company
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2010-12-17
Marketing end 0000-00-00
Substance IRON; GUAIACUM OFFICINALE RESIN; LITHIUM CARBONATE; TOMATO; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Active strength 30 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 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 57520-0272-1 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
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 57520-0272-1 Fibro Relief 120 in 1 BOTTLE CAPSULE 120 1
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded GUAIACUM OFFICINALE RESIN ACTIVE INGREDIENT N0K2Z502R6 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 IRON ACTIVE INGREDIENT E1UOL152H7 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 LITHIUM CARBONATE ACTIVE INGREDIENT 2BMD2GNA4V FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE ACTIVE INGREDIENT HF539G9L3Q FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 TOMATO ACTIVE INGREDIENT Z4KHF2C175 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 GUAIACUM OFFICINALE RESIN ACTIVE MOIETY N0K2Z502R6 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 IRON ACTIVE MOIETY E1UOL152H7 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 LITHIUM CATION ACTIVE MOIETY 8H8Z5UER66 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 MAGNESIUM CATION ACTIVE MOIETY T6V3LHY838 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 TOMATO ACTIVE MOIETY Z4KHF2C175 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 ELYMUS REPENS ROOT INACTIVE INGREDIENT 3IXW0F6P8W FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 EUROPEAN ELDERBERRY INACTIVE INGREDIENT BQY1UBX046 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 LOBELIA INFLATA INACTIVE INGREDIENT 9PP1T3TC5U FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 MARSDENIA CONDURANGO BARK INACTIVE INGREDIENT R23QIR6YBA FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 NYMPHAEA ODORATA ROOT INACTIVE INGREDIENT 69RAZ4C432 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 POWDERED CELLULOSE INACTIVE INGREDIENT SMD1X3XO9M FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 RUMEX CRISPUS ROOT INACTIVE INGREDIENT 9N1RM2S62C FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57520-0272 FIBRO RELIEF (FERRUM METALLICUM, GUAIACUM, LITHIUM CARBONICUM, LYCOPERSICUM ESCULENTUM, MAGNESIA PHOSPHORICA) CAPSULE [APOTHECA COMPANY] 1 Legacy NDC, 1 package rows 20110425_b609950f-7510-4b88-b7d8-c327be0ee96e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 57520-0272-1 57520027201 120 in 1 BOTTLE Historical