Home NDC 55146-009-01 9 Bacterial Detox
Product NDC 55146-009
Requested package NDC 55146-009-01
11-digit product format 551460009
Labeler code 55146
Product ID 55146-009_e28b0fa2-7837-4cc2-8902-6737db0b5b17
Type HUMAN OTC DRUG
Nonproprietary name Baptisia Tinctoria, Dulcamara, Echinacea (Angustifolia), Allium Sativum, Phytolacca Decandra, Apis Mellifica, Arsenicum Album, Belladonna, Chamomilla, Ferrum Phosphoricum, Gelsemium Sempervirens, Lachesis Mutus, Mercurius Solubilis, Pyrogenium
Dosage form LIQUID
Route ORAL
Labeler Biotics Research Corporation
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-06-11
Marketing end 0000-00-00
Substance BAPTISIA TINCTORIA ROOT; SOLANUM DULCAMARA TOP; ECHINACEA ANGUSTIFOLIA; GARLIC; PHYTOLACCA AMERICANA ROOT; APIS MELLIFERA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; MATRICARIA RECUTITA; FERROSOFERRIC PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; RANCID BEEF
Active strength 3 [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; [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 · 10 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 2025-12-14 17:58 UTC · source 2025-12-05 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2024-10-04 04:10 UTC · source 2024-10-03 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 I Inactivated by FDA bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55146-009 9 BACTERIAL DETOX (BAPTISIA TINCTORIA, DULCAMARA, ECHINACEA (ANGUSTIFOLIA), ALLIUM SATIVUM, PHYTOLACCA DECANDRA, APIS MELLIFICA, ARSENICUM ALBUM, BELLADONNA, CHAMOMILLA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, LACHESIS MUTUS, MERCURIUS SOLUBILIS, PYROGENIUM) LIQUID [BIOTICS RESEARCH CORPORATION] 5 Legacy NDC 20241020_46595996-7af9-4de4-848d-61e931dc1929.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 55146-009-01 55146000901 120 mL in 1 BOTTLE, PLASTIC (55146-009-01) 120 ml 2019-06-11 0000-00-00 No No Current