Blood Stop Powder

Manufacturer: MWI (VetOne)
Effective date: 2024-10-25
Label type: OTC ANIMAL DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:43:56

Label at a glance#

ProductBlood Stop Powder

Active ingredientFERROUS SULFATE

Label structure5 sections

Dosage and administration

Apply powder freely to bleeding surface. Repeat as needed. Bandage if necessary.

Storage and handling

Store at controlled room temperature between 15 o -30 o C (59 o -86 o F) Keep container tightly closed. TAKE TIME TO OBSERVE LABEL DIRECTIONS

Label contents#

Full prescribing information#

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Apply powder freely to bleeding surface. Repeat as needed. Bandage if necessary.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

In case of deep or puncture wounds or serious burns, consult veterinarian. If redness, irritation, or swelling persists or increases, discontinue use and consult veterinarian.

COMPONENTS

Ferrous Sulfate • 7H₂O 84.0%, Ammonium Alum 5%, Chloroxylenol 1%, Tannic Acid 1%, In a free-flowing absorbent base. Not sterilized.

For external use only.

STORAGE AND HANDLING SECTION

Store at controlled room temperature between 15^o-30^oC (59^o-86^oF)

Keep container tightly closed.

TAKE TIME TO OBSERVE LABEL DIRECTIONS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

vetone-bsp

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
895952	ferrous sulfate 84 % Topical Powder	PSN	1
895952	ferrous sulfate 840 MG/MG Topical Powder	SCD	1
895952	FeSO4 84 % Topical Powder	SY	1
895952	FESO4 840 MG/MG Topical Powder	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
910c1bd7-67d1-44c7-ad4f-9445f827edcc	Product name	1	20230808

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
86136-014-16	Blood Stop Powder	454 g in 1 JAR	POWDER	454		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
86136-014	BLOOD STOP POWDER (IRON) POWDER [MWI (VETONE)]	1	1 package rows	20241204_281aa864-8f9b-46a5-95d7-8aeeaeabbe1a.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Blood Stop Powder
IRON
FERROUS SULFATE
FERROUS CATION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
86136-014	86136-014-16

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
FERROUS SULFATE	39R4TAN1VT	ACTIM

Source Document#

Source XML

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 · 4 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
FERRUM SULPHURICUM	FERROUS SULFATE	Boiron	3a749d62-0e20-0c15-e063-6394a90ac1a8	2025-07-21		Name fallback generic name: FERROUS SULFATE
FERROUS SULFATE	FERROUS SULFATE	Richmond Pharmaceuticals, Inc.	58dd4f30-980b-44bc-9f8e-8d4626854b91	2024-12-26	Warnings	Name fallback generic name: FERROUS SULFATE
Ferrous Sulfate	FERROUS SULFATE	Richmond Pharmaceuticals Inc.	5514d582-19b5-4f1e-b794-f790afb8211c	2024-12-26	Boxed warning, Warnings	Name fallback generic name: FERROUS SULFATE
Ferrum sulphuricum	FERROUS SULFATE	Boiron	7a4087d8-d054-bbdc-e053-2991aa0ae8cf	2023-11-13		Name fallback generic name: FERROUS SULFATE

Reported adverse events (FAERS/openFDA)#

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