Label: HOOF N HEEL- zinc sulfate, sodium lauryl sulfate liquid

  • NDC Code(s): 15878-214-11, 15878-214-19
  • Packager: H. W. Naylor Company Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 7, 2021

If you are a consumer or patient please visit this version.

  • Active Ingredients

    11.2% (w/v) Zinc Sulfate equivalent to 20% as the Zinc Sulfate Heptahydrate, 2% (w/v) Sodium Lauryl Sulfate

  • Purpose

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

  • Directions

    1. Clean and trim, when necessary, affected hoofs to expose and remove all dead, loose, undermined tissue. Control any bleedinq 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. Tum sheep out in pasture that has been vacant for at least two weeks. Keep separate from nontreated, affected animals.
  • Safety

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

    Livestock remedy. Not for human use.

    For external veterinary use only.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

  • Other Ingredients

    Water

  • Questions?

    www.drnaylor.com

  • Principal Display Panel - 16 ounce bottle

    Dr. Naylor®

    Veterinary Topical Antibacterial

    HOOF n HEEL®

    FOR

    HOOF ROT ● FOOT ROT
    FOULS, FOOT SCALD

    SHEEP, GOATS, CATTLE, DAIRY COWS

    An aid in the treatment of cattle with 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, FOULS, FOOT SCALD
    IN SHEEP, GOATS, CATTLE, DAIRY COWS

    Made in U.S.A.

    H.W. Naylor Company, Inc.

    Morris NY 13808-019

    16 Ounce Bottle Label

  • PRINCIPAL DISPLAY PANEL - 1 Gallon Bottle

    Veterinary Topical Antibacterial

    HOOF n HEEL®

    FOR

    HOOF ROT ● FOOT ROT
    FOULS, FOOT SCALD
    SHEEP, GOATS, CATTLE, DAIRY COWS

    An aid in the treatment of cattle with 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, FOULS, FOOT SCALD
    IN SHEEP, GOATS, CATTLE, DAIRY COWS

    Made in U.S.A.

    H.W. Naylor Company, Inc.

    Morris NY 13808-019

    1 gallon bottle label

  • INGREDIENTS AND APPEARANCE
    HOOF N HEEL  
    zinc sulfate, sodium lauryl sulfate liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:15878-214
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Zinc Sulfate (UNII: 89DS0H96TB) (Zinc Cation - UNII:13S1S8SF37) Zinc Cation100 g  in 1000 mL
    Sodium Lauryl Sulfate (UNII: 368GB5141J) (Lauryl Sulfate - UNII:DIQ16UC154) Sodium Lauryl Sulfate18 g  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:15878-214-11474 mL in 1 BOTTLE
    2NDC:15878-214-193790 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/1964
    Labeler - H. W. Naylor Company Inc. (002080190)
    Establishment
    NameAddressID/FEIBusiness Operations
    H. W. Naylor Company Inc.002080190manufacture, api manufacture