Bartonella Plus

Product NDC
43742-1178
Requested package NDC
43742-1178-1
11-digit product format
437421178
Labeler code
43742
Product ID
43742-1178_bb6dfec2-8050-4897-9862-1e602232b82f
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Montana, Echinacea (Angustifolia), Glycyrrhiza Glabra, Hydrastis Canadensis, Ledum Palustre, Thyroidinum (Suis), Arbutus Andrachne, Apis Mellifica, Arsenicum Album, Cocculus Indicus, Gunpowder, Hepar Sulphuris Calcareum, Kalmia Latifolia, Lac Caninum, Lycopodium Clavatum, Veratrum Album, Aconitum Napellus, Stramonium, Tellurium Metallicum
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-03-16
Marketing end
2025-09-04
Substance
ARNICA MONTANA; ECHINACEA ANGUSTIFOLIA; GLYCYRRHIZA GLABRA; GOLDENSEAL; RHODODENDRON TOMENTOSUM LEAFY TWIG; THYROID, PORCINE; ARBUTUS ANDRACHNE LEAFY SHOOT; APIS MELLIFERA; ARSENIC TRIOXIDE; ANAMIRTA COCCULUS SEED; ACTIVATED CHARCOAL; SULFUR; POTASSIUM NITRATE; CALCIUM SULFIDE; KALMIA LATIFOLIA LEAF; CANIS LUPUS FAMILIARIS MILK; LYCOPODIUM CLAVATUM SPORE; VERATRUM ALBUM ROOT; ACONITUM NAPELLUS; DATURA STRAMONIUM; TELLURIUM
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_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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage43742-117843742-1178-1DDiscontinued by firm2026-10-05

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 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage43742-117843742-1178-1DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1178BARTONELLA PLUS (ARNICA MONTANA, ECHINACEA (ANGUSTIFOLIA), GLYCYRRHIZA GLABRA, HYDRASTIS CANADENSIS, LEDUM PALUSTRE, THYROIDINUM (SUIS), ARBUTUS ANDRACHNE, APIS MELLIFICA, ARSENICUM ALBUM, COCCULUS INDICUS, GUNPOWDER, HEPAR SULPHURIS CALCAREUM, KALMIA LATIFOLIA, LAC CANINUM, LYCOPODIUM CLAVATUM, VERATRUM ALBUM, ACONITUM NAPELLUS, STRAMONIUM, TELLURIUM METALLICUM) LIQUID [DESERET BIOLOGICALS, INC.]2Legacy NDC20210624_8488a241-367d-4ad0-a7b2-292695a7bff0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1178-14374211780130 mL in 1 BOTTLE, DROPPER (43742-1178-1) 30 ml2018-03-162025-09-04NoNoCurrent