Hoofbath Booster HFB50

Manufacturer: DeLaval | WestAgro, Inc. | K Klean dba WestAgro, Inc.
Effective date: 2022-01-04
Label type: OTC ANIMAL DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 22:19:13

Label at a glance#

ProductHoofbath Booster HFB50

Active ingredientHYDROCHLORIC ACID

Label structure15 sections

Storage and handling

STORAGE AND DISPOSAL THOROUGHLY RINSE ALL MEASURING DEVICES AND STORE OUT OF REACH OF CHILDREN. Avoid contamination of food or feed. Avoid storing near heat or open flame. Store in cool, dry place. Keep container tightly closed when not in use. Do not reuse empty container. Rinse container before disposing in a safe manner.

Contacts and useful links#

PhoneLabel contact1-800-424-9300

PhoneLabel contact816-891-7700

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

An aid to prevent hoof rot and hairy heel warts. Reduces the use of copper sulfate.

Ayuda en la prevencion de verruga peluda y gabarro. Diminuye el uso de sulfato de cobre.

SPL UNCLASSIFIED SECTION

Hoofbath Booster HFB50

Concentrated footbath enhancer

Potenciador concentrado para pediluvios

SPL UNCLASSIFIED SECTION

1 2 The hoof care two-step:

First clean then disinfect

El cuidado para pezunas de dos etapes:

en primer lugar limpiar y desinfectar

SPL UNCLASSIFIED SECTION

Contains: cationic surfactant, mineral acid, and Red 40

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

MANTENER FUERA DEL ALCANCE DE LOS NINOS

! DANGER ! PELIGRO

SPL UNCLASSIFIED SECTION

ADDITIONAL INFORMATION ON SAFETY DATA SHEET

SI USTED NO PUEDE LEER ESTA ETIQUETA, POR FAVOR PIDA A ALGUIEN MAS QUE SE LA LEA ANTES DE USAR ESTE PRODUCTO

READ AND UNDERSTAND ALL INSTRUCTIONS BEFORE USING THIS PRODUCT

WARNINGS AND PRECAUTIONS SECTION

CORROSIVE. Causes severe burns to skin, eyes, and mucous membranes. Avoid contact with skin, eyes, and mucous membranes. Wear protective apron, gloves, and goggles, or face shield when handling this product. Wash thoroughly after handling this product. Use this product with adequate ventilation.

Harmful or fatal if swallowed. Swallowing product will cause severe burns to lining of throat and stomach. Do not take internally. Do not taste or swallow.

Flammable liquid and vapor. Keep away from heat, sparks, and flame. Keep container closed. Use only with adequate ventilation.

Do not mix this product with products containing chlorine. Deadly chlorine gas will form immediately.

FIRE AND EXPLOSION HAZARD: This product can react and cause damage to soft metals such as aluminum, copper, brass, or zinc (galvanized) to product flammable, potentially explosive, gas.

SPL UNCLASSIFIED SECTION

FIRST AID

If in eyes: Hold eye open and rinse slowly and gently with water for 15 - 20 minutes. Remove contact lenses, if present, after first 5 minutes, and then continue rinsing. Call a Poison Control Center or doctor for treatment advice.

If swallowed: Immediatel call Poison Control Center or doctor for treatment advice. Give person large amounts of milk or water if able to swallow. Do not induce vomiting unless told to do so by the Poison Control Center or doctor. Do not give anything by mouth to an unconscious person.

If on skin or clothing: Take off contaminated clothing. Rinse skin immediately with plenty of water for 15 - 20 minutes. Call Poison Control Center or doctor for treatment advice. Wash clothes before reuse.

In inhaled: Immediately move person to fresh air. If person is not breathing, immediately call 911 or an ambulance, then give artificial respiration, preferable mouth-to-mouth, if possible. Call a Poison Control Center or doctor for treatment advice.

STORAGE AND HANDLING SECTION

STORAGE AND DISPOSAL

THOROUGHLY RINSE ALL MEASURING DEVICES AND STORE OUT OF REACH OF CHILDREN. Avoid contamination of food or feed. Avoid storing near heat or open flame. Store in cool, dry place. Keep container tightly closed when not in use. Do not reuse empty container. Rinse container before disposing in a safe manner.

SPL UNCLASSIFIED SECTION

CHEM-TREC EMERGENCY NUMBER: 1-800-424-9300

INSTRUCTIONS FOR USE SECTION

USE DIRECTIONS

NOT FOR HUMAN USE. Do not use at full strength. Dilute according to directions. Read and follow label instructions carefully. Consult a veterinarian for proper diagnosis of lameness before using this product. For best results, use this product as a part of a complete hoof care program.

Hoofbath Booster HFB50 is a footbath additive specially developed to enhance the efficacy of copper and zinc sulfate. It allows for reduction of consumption of copper sulfate in half.

Footbath Dilutions: Footbath dilutions are intended for use on 200 cows, after which it is recommended that the footbath solution be discarded and replaced with a fresh footbath solution.

Mix thoroughly 1 quart Hoofbath Booster HFB50 with 12.5 pounds of copper sulfate (1/4 of a 50 pound bag). Dilute to 50 gallons.
If footbath capacity is unknown, use the following formula: Inside Length (inches) x Inside Width (inches) x Fluid Height (inches) / 231 = Gallon Capacity of Footbath

WARNINGS SECTION

CORROSIVE

DOT SHIPPING NAME

UN2920

Corrosive liquid, flammable, n.o.s. (Hydrochloric Acid, Quaternary Ammonium Compound, Ethanol), 8(3), PG II

SPL UNCLASSIFIED SECTION

Manufactured for: DeLaval, Inc.
11100 N. Congress Avenue
Kansas City, MO 64153
Phone: 816-891-7700
Manufactured by: WestAgro, Inc.
©2018, Made in USA

SPL UNCLASSIFIED SECTION

NET CONTENTS:

LOT NO.:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
HYDROCHLORIC ACID	ACTIVE INGREDIENT	QTT17582CB	2
HYDROCHLORIC ACID	ACTIVE MOIETY	QTT17582CB	2
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	2
AMMONIA N-13	INACTIVE INGREDIENT	9OQO0E343Z	2
DIDECYLDIMETHYLAMMONIUM CHLORIDE	INACTIVE INGREDIENT	JXN40O9Y9B	2
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	2
N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18)	INACTIVE INGREDIENT	9U1Q4T4ZYS	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	2

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Hoofbath Booster HFB50
Hydrochloric Acid
WATER
N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18)
DIDECYLDIMONIUM CHLORIDE
AMMONIA N-13
FD&C RED NO. 40
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55756-133	55756-133-02, 55756-133-01

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
HYDROCHLORIC ACID	QTT17582CB	ACTIB
WATER	059QF0KO0R	IACT
N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18)	9U1Q4T4ZYS	IACT
DIDECYLDIMONIUM CHLORIDE	JXN40O9Y9B	IACT
AMMONIA N-13	9OQO0E343Z	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
ALCOHOL	3K9958V90M	IACT

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 2 · 87 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, EMULSION / INTRAVENOUS		520 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / ORAL		681 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	JELLY / VAGINAL	NA		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAVASCULAR	100 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	GUM, CHEWING / BUCCAL		48 mg	Exact identifier — unii candidate 28 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	ELIXIR / ORAL	12.5 mg/5ml		Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / INTRAVENOUS		400 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SHAMPOO / TOPICAL		714 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAMUSCULAR		1491 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / TRANSDERMAL	49.37 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	TABLET / BUCCAL	0.01 mg		Exact identifier — unii candidate 28 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	CAPSULE, EXTENDED RELEASE / ORAL		1 mg	Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / TRANSDERMAL		7360 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	SOLUTION / ORAL		38 mg	Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, METERED / NASAL	70 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, METERED / RESPIRATORY (INHALATION)		26664 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	ELIXIR / ORAL		13675 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / INTRAVENOUS		99 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / DENTAL	1.8 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	CONCENTRATE / ORAL	0.04 mg/1ml		Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL, METERED / TRANSDERMAL		3675 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	TABLET / SUBLINGUAL	NA		Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / TOPICAL		9971 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, FOAM / TOPICAL		4504 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAVENOUS	92 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SYRUP / ORAL		21000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE, EXTENDED RELEASE / ORAL		8 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TOPICAL		3633 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / ORAL	210 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / SUBCUTANEOUS	6.1 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	TABLET / ORAL		7 mg	Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL, METERED / TOPICAL		541 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	SPONGE / TOPICAL	NA		Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SWAB / TOPICAL		2250 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / INTRAVENOUS		4000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	CAPSULE, COATED, EXTENDED RELEASE / ORAL	NA		Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / INTRAVESICAL		7892 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	POWDER, FOR SUSPENSION / ORAL		3 mg	Exact identifier — unii candidate 28 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	SYRUP / ORAL		3 mg	Exact identifier — unii candidate 28 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	CAPSULE / ORAL		16 mg	Exact identifier — unii candidate 28 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	SOLUTION / DENTAL	NA		Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TRANSDERMAL	90 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / TOPICAL		2445 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	POWDER, FOR SOLUTION / ORAL	0.33 mg/5ml		Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL / TOPICAL		561 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	CAPSULE, DELAYED RELEASE PELLETS / ORAL	0.02 mg		Exact identifier — unii candidate 28 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	CAPSULE, LIQUID FILLED / ORAL		1 mg	Exact identifier — unii candidate 28 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	CAPSULE, COATED PELLETS / ORAL	NA		Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / INTRAVENOUS		6405 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / BUCCAL	679 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	TABLET, EXTENDED RELEASE / ORAL	2.22 mg		Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / RECTAL		898 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / INTRAMUSCULAR		400 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, SPRAY / RESPIRATORY (INHALATION)	35.75 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE / ORAL		882 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	SUSPENSION / ORAL	100 mg/5ml		Exact identifier — unii candidate 28 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	TABLET, COATED / ORAL	0.1 mg		Exact identifier — unii candidate 28 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / RESPIRATORY (INHALATION)	5 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / SUBLINGUAL		397 mg	Exact identifier — unii candidate 59 equally ranked IID candidates

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 · 5 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Muriaticum acidum	HYDROCHLORIC ACID	Boiron	8643bc58-bb0e-5c79-e053-2991aa0a02ae	2026-05-19	Warnings	Name fallback generic name: HYDROCHLORIC ACID
Muriaticum acidum	HYDROCHLORIC ACID	Boiron	8643994f-4e13-4572-e053-2991aa0a5b78	2023-11-14		Name fallback generic name: HYDROCHLORIC ACID
Muriaticum acidum	HYDROCHLORIC ACID	Boiron	6907bbfe-caa5-2ce4-e053-2991aa0ade8d	2023-11-14		Name fallback generic name: HYDROCHLORIC ACID
Muriaticum acidum	HYDROCHLORIC ACID	Boiron	8643c518-13b2-658a-e053-2a91aa0ac5ed	2023-11-14		Name fallback generic name: HYDROCHLORIC ACID
Muriaticum acidum	HYDROCHLORIC ACID	Boiron	8643e30e-1f47-09f1-e053-2991aa0ac2de	2023-11-14		Name fallback generic name: HYDROCHLORIC ACID

Reported adverse events (FAERS/openFDA)#

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