Home NDC 43857-0517-1 Amoebatox
Product NDC 43857-0517
Requested package NDC 43857-0517-1
11-digit product format 438570517
Labeler code 43857
Product ID 43857-0517_f5ad6638-3a2d-45a7-99c9-dfb398ed7a02
Type HUMAN OTC DRUG
Nonproprietary name Triticum Aestivum, Baptisia Tinctoria, Capsicum Annuum, Fragaria Vesca, Hamamelis Virginiana, Quassia Amara, Senna, Hydrastis Canadensis, Podophyllum Peltatum, Hepar Bovine, Pancreas Suis, Spleen (Bovine), Belladonna, Cinchona Officinalis, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Giardia Lamblia, Entamoeba Histolytica
Dosage form LIQUID
Route ORAL
Labeler BioActive Nutritional, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-08-06
Marketing end 2024-12-09
Substance TRITICUM AESTIVUM WHOLE; BAPTISIA TINCTORIA ROOT; CAPSICUM; ALPINE STRAWBERRY; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; QUASSIA AMARA WOOD; SENNA LEAF; GOLDENSEAL; PODOPHYLLUM; BEEF LIVER; SUS SCROFA PANCREAS; BOS TAURUS SPLEEN; ATROPA BELLADONNA; CINCHONA OFFICINALIS BARK; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; ENTAMOEBA HISTOLYTICA; GIARDIA LAMBLIA
Active strength 1 [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_X]/mL; [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
NDC exclude flag No
Listing certified through 0000-00-00
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43857-0517-1 43857051701 30 mL in 1 BOTTLE, DROPPER (43857-0517-1) 30 ml 2019-08-06 2024-12-09 No No Current