Dosage and administration
Treatment 1. Add entire contents to 20 gallons of water. 2. Restrain animals in foot bath solution for one hour . Preventative 1. Add entire contents to 40 gallons of water. 2. Use as daily walk through.
HOOF n HEEL
- Manufacturer
- H. W. Naylor Company Inc.
- Effective date
- 2021-12-08
- Label type
- OTC ANIMAL DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 02:41:11
Label at a glance#
ProductHOOF n HEEL
Active ingredientZinc Sulfate, Sodium Lauryl Sulfate
Label structure8 sections
Contacts and useful links#
Websitewww.drnaylor.com
www.drnaylor.com
www.drnaylor.comLabel contents#
Full prescribing information#
Active Ingredients
100% ACTIVE INGREDIENTS: Zinc Sulfate, monohydrate 86.7%
Sodium Lauryl Sulfate 13.3%
When reconstituted with 20 gallons of water, contains 11.2% Zinc Sulfate (Equivalent to 20% Zinc Sulfate as the heptahydrate) and 2% Sodium Lauryl Sulfate
Purpose
An aid in the treatment of cattle with foot rot due to organisms susceptible to zinc sulfate.
Directions
Treatment
1. Add entire contents to 20 gallons of water.
2. Restrain animals in foot bath solution for one hour.
Preventative
1. Add entire contents to 40 gallons of water.
2. Use as daily walk through.
CAUTION:
For Veterinary external use only. Livestock remedy. Not for human use. Avoid product or solution contact with eyes. Nursing lambs or kids accompanying mothers should be monitored to forestall any trampling or immersion when attempting to nurse. If redness, irritations, or swelling persists or increases, consult a veterinarian.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of the reach of children.
Other Ingredients
Add water for reconstitution
Questions?
Principal Display Panel
NEW
Dr. Naylor®
HOOF 'n HEEL®
POWDER CONCENTRATE
HOOF ROT — FOOT ROT
FOULS - FOOT SCALD
IN SHEEP, GOATS, CATTLE, DAIRY COWS
An aid in the treatment of cattle with foot rot due to organisms susceptible to zinc sulfate.
*NO HOOF TRIMMING
*NON TOXIC COMPARED TO COPPER SULFATE & FORMALDEHYDE
*EASY TREATMENT METHOD*ECONOMICAL
*NO FUMES. ODORLESS. COLORLESS
*DOES NOT STAIN OR AFFECT WOOL*REUSEABLE. STABLE. WON'T DETERIORATE. UNPALATABLE.
*DOES NOT DISCOLOR, HARDEN, SHRINK OR MAKE HOOF BRITTLE
SEE PACKAGE INSERT FOR COMPLETE DIRECTIONS
Contents: 11.9 kg (26 lbs. 5 oz.)
Made in U.S.A.
H.W. NAYLOR CO., Inc.
Morris NY 13808-0190
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| ZINC CATION Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f47a510b-6679-4664-b2d6-47b5c4afe7cc | Product name | 4 | 20260217 |
| 030ce964-9b2d-45aa-b5d3-f78ce03ef61c | Product name | 2 | 20250515 |
| 0306390c-dd77-4363-afe0-63c58088b2a1 | Product name | 1 | 20220120 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| 190f2a5b-bbc8-65c7-fcb0-97891307b917 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 15878-514-15 | HOOF n HEEL | 11.9 kg in 1 CARTON | CONCENTRATE | 11.9 | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Sodium Lauryl Sulfate | ACTIVE INGREDIENT | 368GB5141J | 2 | |
| Zinc Sulfate | ACTIVE INGREDIENT | 89DS0H96TB | 2 | |
| Lauryl Sulfate | ACTIVE MOIETY | DIQ16UC154 | 2 | |
| Zinc Cation | ACTIVE MOIETY | 13S1S8SF37 | 2 |
Products#
Every source-derived product name is available through these pages.
- HOOF n HEEL
- Zinc Sulfate, Sodium Lauryl Sulfate
- Zinc Sulfate
- Zinc Cation
- Sodium Lauryl Sulfate
- Lauryl Sulfate
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 15878-514 | 15878-514-15 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Zinc Sulfate | 89DS0H96TB | ACTIM |
| Sodium Lauryl Sulfate | 368GB5141J | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| ZINC SULFATE | ZINC SULFATE | Camber Pharmaceuticals, Inc. | 49698d00-f44b-4b1f-ae34-6b9067911757 | 2026-03-04 | Warnings, Adverse reactions | ZINC SULFATE |
| Zinc Sulfate | ZINC SULFATE | Piramal Critical Care Inc. | dfa8a859-c285-17a3-e053-2a95a90a9343 | 2025-10-07 | Warnings, Adverse reactions | ZINC SULFATE |
| Zinc Sulfate | ZINC SULFATE | Piramal Critical Care Inc. | 0b6078d9-624c-e162-e063-6394a90a147d | 2024-12-17 | Warnings, Adverse reactions | ZINC SULFATE |
| Zinc sulfate | ZINC SULFATE | Somerset Therapeutics, LLC | c9d45d0e-a165-4112-81f9-c0e455572ecf | 2024-07-18 | Warnings, Adverse reactions | ZINC SULFATE |
| Zinc Sulfate | ZINC SULFATE | Gland Pharma Limited | 8f354f0a-4e10-4e4e-b86c-49d97cbd631d | 2023-09-07 | Warnings, Adverse reactions | ZINC SULFATE |
| zinc sulfate | ZINC SULFATE | Zydus Lifesciences Limited | 74d8d07b-cfd9-4262-b689-fea12673bbd1 | 2023-08-31 | ZINC SULFATE | |
| Zinc Sulfate | ZINC SULFATE | Fresenius Kabi USA, LLC | 37d54dcd-b720-4168-bfb2-c8f381466aac | 2023-01-04 | Warnings, Adverse reactions | ZINC SULFATE |
| Zinc Sulfate | ZINC SULFATE | American Regent, Inc. | 4b528c88-07a0-4dce-84c6-ccd32555bbff | 2020-10-01 | Warnings, Adverse reactions | ZINC SULFATE |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.