ULCERFACTOR

Manufacturer: Immuvet, Inc. | Amino Cell, Inc
Effective date: 2025-11-04
Label type: OTC ANIMAL DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:37:21

Label at a glance#

ProductULCERFACTOR

Active ingredientARTEMISIA VULGARIS ROOT, LYTTA VESICATORIA, MILK THISTLE, CHELIDONIUM MAJUS, LYCOPODIUM CLAVATUM SPORE

Label structure7 sections

Dosage and administration

Orally administer 10 cc for the first 20 days, thereafter 10 cc every other day. Shake 10 times before using.

Label contents#

Full prescribing information#

PURPOSE

OTC - PURPOSE SECTION

Helps to reduce the incidence and severity of chronic gastritis and gastric ulcers in horses.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Orally administer 10 cc for the first 20 days, thereafter 10 cc every other day. Shake 10 times before using.

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Artemisia Vulgaris 30c HPUS
Cantharis 30c HPUS
Carduus Marianus 30c HPUS
Chelidonium Majus 30c HPUS
Lycopodium 30c HPUS

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Distilled water, Alcohol 3%

WARNINGS

WARNINGS SECTION

Do not use if seal is broken.
For Oral Veterinary Use Only.
Not for use in Horses intended for food.
If problems persist, contact a veterinarian.
Keep out of reach of children.

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0864591000180	GTIN-13: 0864591000180 EAN-13: 0864591000180 GTIN-12: 864591000180 UPC-A: 864591000180 GTIN storage (14 digits): 00864591000180	Ulcerfactor 2022 homeopathic SPL.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59517-1810-4	ULCERFACTOR	200 mL in 1 BOTTLE	LIQUID	200		3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

ULCERFACTOR
ARTEMISIA VULGARIS, LYTTA VESICATORIA, MILK THISTLE, CHELIDONIUM MAJUS, LYCOPODIUM CLAVATUM
ARTEMISIA VULGARIS ROOT
LYTTA VESICATORIA
MILK THISTLE
ALCOHOL
WATER
CHELIDONIUM MAJUS
LYCOPODIUM CLAVATUM SPORE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59517-1810	59517-1810-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ARTEMISIA VULGARIS ROOT	32MP823R8S	ACTIB
LYTTA VESICATORIA	3Q034RO3BT	ACTIB
MILK THISTLE	U946SH95EE	ACTIB
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
CHELIDONIUM MAJUS	7E889U5RNN	ACTIB
LYCOPODIUM CLAVATUM SPORE	C88X29Y479	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
2	2024-12-23	full-release	2026-06-01 02:29:50

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Artemisia vulgaris	ARTEMISIA VULGARIS ROOT	Boiron	253c9d92-7555-4429-e063-6394a90a52f1	2024-10-24		Name fallback generic name: ARTEMISIA VULGARIS ROOT
Artemisia vulgaris	ARTEMISIA VULGARIS ROOT	Boiron	6c316c2c-ce7b-a5b2-e053-2991aa0a9743	2024-10-24		Name fallback generic name: ARTEMISIA VULGARIS ROOT

Reported adverse events (FAERS/openFDA)#

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