FDA.reportPublic FDA data

Stop 20-pm

Manufacturer
Immuvet, Inc. | Amino Cell, Inc
Effective date
2025-10-06
Label type
OTC ANIMAL DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:37:00

Label at a glance#

ProductStop 20-pm
Active ingredientBRYONIA ALBA ROOT, PARIS QUADRIFOLIA, PHOSPHORUS, ANTIMONY POTASSIUM TARTRATE, ACONITUM NAPELLUS, POTASSIUM CARBONATE, MERCURIUS SOLUBILIS
Label structure7 sections

Dosage and administration

Orally administer 10 cc in the morning on an empty stomach 30 minutes before feeding. For the first 20 days, do not breeze, gallop, or undergo rigorous training. Shake 10 times before using.

Label contents#

Full prescribing information#

PURPOSE

OTC - PURPOSE SECTION

Helps to reduce the incidence and severity of EIPH (bleeding) in performance horses.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Orally administer 10 cc in the morning on an empty stomach 30 minutes before feeding. For the first 20 days, do not breeze, gallop, or undergo rigorous training. Shake 10 times before using.

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Argentum Nitricum 200x HPUS
Allium Sativa 12x HPUS
Phosphorus 200x HPUS
Ipecacuanha 30x HPUS 

Cinnamomum 12x HPUS }

Pulsatilla 12x HPUS
Natrum Sulphuricum 12x HPUS
Rumex Crispus 30x 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

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130864591000166GTIN-13: 0864591000166
EAN-13: 0864591000166
GTIN-12: 864591000166
UPC-A: 864591000166
GTIN storage (14 digits): 00864591000166		stop 20 pm 2022 homeopathic.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59517-1730-4Stop 20-pm200 mL in 1 BOTTLELIQUID2002

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59517-173059517-1730-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BRYONIA ALBA ROOTT7J046YI2BACTIB
PARIS QUADRIFOLIAPME3ETQ5WQACTIB
PHOSPHORUS27YLU75U4WACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
ANTIMONY POTASSIUM TARTRATEDL6OZ476V3ACTIB
ACONITUM NAPELLUSU0NQ8555JDACTIB
POTASSIUM CARBONATEBQN1B9B9HAACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12022-08-29full-release2026-06-01 02:18:05

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 · 14 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BryoniaBRYONIA ALBA ROOTBoiron8489ca49-bfdf-0df7-e053-2991aa0af54f2026-01-06Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoiron848a2761-244f-3614-e053-2a91aa0aec852026-01-05Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoiron8502566a-3451-f2bb-e053-2991aa0a13a42026-01-05Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoiron85023f1e-dfb2-3261-e053-2991aa0aa9f72026-01-05Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoiron8502ac84-1022-e92d-e053-2991aa0a38bc2026-01-05Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoironb23a2d30-79fe-11e6-a1b8-424c583030312026-01-05Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoiron848996a1-46e4-035f-e053-2a91aa0a58222026-01-05Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoiron848970a6-6bcc-64f4-e053-2a91aa0ac1482026-01-05Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoiron8502ac84-100a-e92d-e053-2991aa0a38bc2026-01-05Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoiron848a1836-b86a-fc68-e053-2991aa0af6a52026-01-02Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoiron85027590-d80e-911f-e053-2a91aa0abf8b2026-01-02Name fallback
generic name: BRYONIA ALBA ROOT
BryoniaBRYONIA ALBA ROOTBoiron8489d328-17e3-317f-e053-2991aa0a87a92026-01-02Name fallback
generic name: BRYONIA ALBA ROOT
Bryonia Alba 200ckBRYONIA ALBA ROOTSEVENE USAc8d49969-f04f-1605-e053-2a95a90a2fb32025-02-11WarningsName fallback
generic name: BRYONIA ALBA ROOT
Bryonia Alba 30cBRYONIA ALBA ROOTSEVENE USA4c742c22-5ff6-4197-ae38-2ed8f9e0b6932024-01-23WarningsName fallback
generic name: BRYONIA ALBA ROOT

Reported adverse events (FAERS/openFDA)#

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