FDA.reportPublic FDA data

HOOF n HEEL

Manufacturer
H. W. Naylor Company Inc.
Effective date
2025-12-10
Label type
OTC ANIMAL DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:45:32

Label at a glance#

ProductHOOF n HEEL
Active ingredientZinc Sulfate, Sodium Lauryl Sulfate
Label structure7 sections

Dosage and administration

Clean and trim, when necessary, affected hoofs to expose and remove all dead, loose, undermined tissue. Control any bleeding before treating with Dr. Naylor® HOOF 'n HEEL®. Slowly squirt Dr. Naylor® HOOF 'n HEEL® on lesion, covering and saturating it and surrounding area thoroughly while holding hoof inverted - Permit it to penetrate before releasing animal. Foot may be wet pack bandaged or soaked to enhance heali...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

11.2% (w/v) Zinc Sulfate equivalent to 20% as the Zinc Sulfate Heptahydrate, 2% (w/v) Sodium Lauryl Sulfate in a cleansing penetrating aqueous base.

Purpose

OTC - PURPOSE SECTION

An aid in the treatment of foot rot due to organisms susceptible to zinc sulfate.

Directions

DOSAGE & ADMINISTRATION SECTION

  1. Clean and trim, when necessary, affected hoofs to expose and remove all dead, loose, undermined tissue. Control any bleeding before treating with Dr. Naylor® HOOF 'n HEEL®.
  2. Slowly squirt Dr. Naylor® HOOF 'n HEEL® on lesion, covering and saturating it and surrounding area thoroughly while holding hoof inverted - Permit it to penetrate before releasing animal. Foot may be wet pack bandaged or soaked to enhance healing - HOOF'n HEEL® is re-usable and stable.
  3. Treat twice daily until healing results.
  4. Retain animal in a clean, dry area while it is undergoing treatment. After completion of treatment, turn out in pasture that has been vacant for at least two weeks. Keep separate from nontreated, affected animals.

Safety

GENERAL PRECAUTIONS SECTION

CAUTION: lf redness, irritation or swelling persists or increases consult veterinarian.

Livestock remedy. Not for human use.

For external veterinary use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Principal Display Panel - 16 ounce bottle

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dr. Naylor®

Veterinary Topical Antibacterial

HOOF 'n HEEL®

FOR

HOOF ROT ● FOOT ROT
THRUSH, FOOT SCALD
HORSES, SHEEP, GOATS, CATTLE, DAIRY COWS

An aid in the treatment of foot rot due to organisms susceptible to zinc sulfate.

Dr. NAYLOR® Hoof 'n Heel®:
• Pleasant to use - not sticky or messy
• Does not cause hoof to become discolored, hard, brittle or shrink.
• Colorless. Does not stain or affect wool.
• Painless. No fumes. Non-toxic.
• No residues. No withholding.
• Economical. Treats many hoofs.

Net Contents:
16 fl oz. (1 pt) (474 ml)

FIGHT HOOF ROT INFECTION
FOOT ROT, HOOF ROT, THRUSH, FOOT SCALD
IN HORSES, SHEEP, GOATS, CATTLE, DAIRY COWS

Made in U.S.A.

H.W. Naylor Company, Inc.

Morris NY 13808-0190

16 Ounce Bottle Label16 Ounce Bottle Label

PRINCIPAL DISPLAY PANEL - 1 Gallon Bottle

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Veterinary Topical Antibacterial

HOOF 'n HEEL®

FOR

HOOF ROT ● FOOT ROT
THRUSH, FOOT SCALD
HORSES, SHEEP, GOATS, CATTLE, DAIRY COWS

An aid in the treatment of foot rot due to organisms susceptible to zinc sulfate.

Dr. NAYLOR® Hoof 'n Heel®:
• Pleasant to use - not sticky or messy
• Does not cause hoof to become discolored, hard, brittle or shrink.
• Colorless. Does not stain or affect wool.
• Painless. No fumes. Non-toxic.
• No residues. No withholding.
• Economical. Treats many hoofs.

Net Contents:
1 Gallon (3.79 L)

FIGHT HOOF ROT INFECTION
FOOT ROT, HOOF ROT, THRUSH, FOOT SCALD
IN HORSES, SHEEP, GOATS, CATTLE, DAIRY COWS

Made in U.S.A.

H.W. Naylor Company, Inc.

Morris NY 13808-0190

1 gallon bottle label1 gallon bottle label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130032584945156GTIN-13: 0032584945156
EAN-13: 0032584945156
GTIN-12: 032584945156
UPC-A: 032584945156
GTIN storage (14 digits): 00032584945156		HHP-Rev02-24.jpg
BarcodeEAN-130032584945163GTIN-13: 0032584945163
EAN-13: 0032584945163
GTIN-12: 032584945163
UPC-A: 032584945163
GTIN storage (14 digits): 00032584945163		HHG-Rev05-25.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15878-214-11HOOF n HEEL474 mL in 1 BOTTLELIQUID4744
15878-214-19HOOF n HEEL3790 mL in 1 BOTTLELIQUID37904

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Sodium Lauryl SulfateACTIVE INGREDIENT368GB5141J2
Zinc SulfateACTIVE INGREDIENT89DS0H96TB2
Lauryl SulfateACTIVE MOIETYDIQ16UC1542
Zinc CationACTIVE MOIETY13S1S8SF372
WaterINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
15878-21415878-214-11, 15878-214-19

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Zinc Sulfate89DS0H96TBACTIM
Sodium Lauryl Sulfate368GB5141JACTIB
Water059QF0KO0RIACT

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 · 8 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ZINC SULFATEZINC SULFATECamber Pharmaceuticals, Inc.49698d00-f44b-4b1f-ae34-6b90679117572026-03-04Warnings, Adverse reactionsName fallback
generic name: ZINC SULFATE
Zinc SulfateZINC SULFATEPiramal Critical Care Inc.dfa8a859-c285-17a3-e053-2a95a90a93432025-10-07Warnings, Adverse reactionsName fallback
generic name: ZINC SULFATE
Zinc SulfateZINC SULFATEPiramal Critical Care Inc.0b6078d9-624c-e162-e063-6394a90a147d2024-12-17Warnings, Adverse reactionsName fallback
generic name: ZINC SULFATE
Zinc sulfateZINC SULFATESomerset Therapeutics, LLCc9d45d0e-a165-4112-81f9-c0e455572ecf2024-07-18Warnings, Adverse reactionsName fallback
generic name: ZINC SULFATE
Zinc SulfateZINC SULFATEGland Pharma Limited8f354f0a-4e10-4e4e-b86c-49d97cbd631d2023-09-07Warnings, Adverse reactionsName fallback
generic name: ZINC SULFATE
zinc sulfateZINC SULFATEZydus Lifesciences Limited74d8d07b-cfd9-4262-b689-fea12673bbd12023-08-31Name fallback
generic name: ZINC SULFATE
Zinc SulfateZINC SULFATEFresenius Kabi USA, LLC37d54dcd-b720-4168-bfb2-c8f381466aac2023-01-04Warnings, Adverse reactionsName fallback
generic name: ZINC SULFATE
Zinc SulfateZINC SULFATEAmerican Regent, Inc.4b528c88-07a0-4dce-84c6-ccd32555bbff2020-10-01Warnings, Adverse reactionsName fallback
generic name: ZINC SULFATE

Reported adverse events (FAERS/openFDA)#

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