Home NDC 44911-0510-1 Infectistat
Product NDC 44911-0510
Requested package NDC 44911-0510-1
11-digit product format 449110510
Labeler code 44911
Product ID 44911-0510_51e182c6-26b2-45a4-b59e-0f72551996f2
Type HUMAN OTC DRUG
Nonproprietary name Baptisia Tinctoria, Echinacea (Angustifolia), Lobelia Inflata, Lomatium Dissectum, Hydrastis Canadensis, Lung (Suis), Phytolacca Decandra, Symphytum Officinale, Aconitum Napellus, Arsenicum Album, Belladonna, Bryonia (Alba), Causticum, Eupatorium Perfoliatum, Ferrum Phosphoricum, Gelsemium Sempervirens, Hypericum Perforatum, Kali Carbonicum, Lachesis Mutus, Natrum Sulphuricum, Phosphorus, Pulsatilla (Pratensis), Rhus Tox, Silicea, Sulphur, Pyrogenium
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-09-13
Marketing end 2025-03-31
Substance ACONITUM NAPELLUS; ANEMONE PRATENSIS; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; CAUSTICUM; COMFREY ROOT; ECHINACEA ANGUSTIFOLIA; EUPATORIUM PERFOLIATUM FLOWERING TOP; FERROSOFERRIC PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; GOLDENSEAL; HYPERICUM PERFORATUM; LACHESIS MUTA VENOM; LOBELIA INFLATA; LOMATIUM DISSECTUM ROOT; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; POTASSIUM CARBONATE; RANCID BEEF; SILICON DIOXIDE; SODIUM SULFATE; SULFUR; SUS SCROFA LUNG; TOXICODENDRON PUBESCENS LEAF
Active strength 12 [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_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
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 44911-0510 44911-0510-1 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 44911-0510 44911-0510-1 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 44911-0510-1 44911051001 30 mL in 1 BOTTLE, DROPPER (44911-0510-1) 30 ml 2019-09-13 2025-03-31 No No Current