Home NDC 55146-010 10 Parasite Detox
Product NDC 55146-010
11-digit product format 551460010
Labeler code 55146
Product ID 55146-010_e57f2936-86f4-4532-8576-79de5df2f84d
Type HUMAN OTC DRUG
Nonproprietary name Carduus Marianus, Chelidonium Majus, Cina, Sabadilla, Teucrium Marum, Terebinthina, Thyroidinum (Suis), Spigelia Anthelmia, Apis Mellifica, Baryta Carbonica, Calcarea Carbonica, Ferrum Muriaticum, Natrum Muriaticum, Silicea, Sulphur
Dosage form LIQUID
Route ORAL
Labeler Biotics Research Corporation
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-06-11
Marketing end 0000-00-00
Substance MILK THISTLE; CHELIDONIUM MAJUS; ARTEMISIA CINA PRE-FLOWERING TOP; SCHOENOCAULON OFFICINALE SEED; TEUCRIUM MARUM; TURPENTINE OIL; SUS SCROFA THYROID; SPIGELIA ANTHELMIA; APIS MELLIFERA; BARIUM CARBONATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; FERRIC CHLORIDE HEXAHYDRATE; SODIUM CHLORIDE; SILICON DIOXIDE; SULFUR
Active strength 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC exclude flag No
Listing certified through 2021-12-31
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 · 20 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 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 55146-010-01 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 55146-010-01 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…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 55146-010-01 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 55146-010-01 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 55146-010-01 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 55146-010-01 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 55146-010-01 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 55146-010-01 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 55146-010-01 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 55146-010-01 I Inactivated by FDA bd6a592717d7…303034d00443…
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 Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55146-010 10 PARASITE DETOX (CARDUUS MARIANUS, CHELIDONIUM MAJUS, CINA, SABADILLA, TEUCRIUM MARUM, TEREBINTHINA, THYROIDINUM (SUIS), SPIGELIA ANTHELMIA, APIS MELLIFICA, BARYTA CARBONICA, CALCAREA CARBONICA, FERRUM MURIATICUM, NATRUM MURIATICUM, SILICEA, SULPHUR) LIQUID [BIOTICS RESEARCH CORPORATION] 4 Legacy NDC 20241020_d079194e-93f2-4c9b-98af-bdd10c8ef7b3.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 55146-010-01 55146001001 120 mL in 1 BOTTLE, PLASTIC (55146-010-01) 120 ml 2019-06-11 0000-00-00 No No Current