Venoforce

Product NDC
43857-0463
Requested package NDC
43857-0463-1
11-digit product format
438570463
Labeler code
43857
Product ID
43857-0463_25558fd8-03f7-41b0-9314-12a13705461d
Type
HUMAN OTC DRUG
Nonproprietary name
Aesculus Hippocastanum, Collinsonia Canadensis, Echinacea (Angustifolia), Hamamelis Virginiana, Pulsatilla (Vulgaris), Arnica Montana, Carbo Vegetabilis, Graphites, Hydrofluoricum Acidum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Paeonia Officinalis, Sepia
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-09-21
Marketing end
0000-00-00
Substance
HORSE CHESTNUT; COLLINSONIA CANADENSIS ROOT; ECHINACEA ANGUSTIFOLIA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; ANEMONE PULSATILLA; ARNICA MONTANA; ACTIVATED CHARCOAL; GRAPHITE; HYDROFLUORIC ACID; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PAEONIA OFFICINALIS ROOT; SEPIA OFFICINALIS JUICE
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
NDC exclude flag
No
Listing certified through
2020-12-31
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 packagepackage43857-046343857-0463-1DDiscontinued 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 · 2 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 packagepackage43857-046343857-0463-1DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage43857-046343857-0463-1DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

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
43857-0463VENOFORCE I (AESCULUS HIPPOCASTANUM, COLLINSONIA CANADENSIS, ECHINACEA (ANGUSTIFOLIA), HAMAMELIS VIRGINIANA, PULSATILLA (VULGARIS), ARNICA MONTANA, CARBO VEGETABILIS, GRAPHITES, HYDROFLUORICUM ACIDUM, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PAEONIA OFFICINALIS, SEPIA) LIQUID [BIOACTIVE NUTRITIONAL, INC.]2Legacy NDC20241020_2ff885ce-08f8-4c7f-8aa5-7efd809643b5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43857-0463-14385704630130 mL in 1 BOTTLE, DROPPER (43857-0463-1) 30 ml2017-09-210000-00-00NoNoCurrent