Label: KERATEX KHG- aluminum stearate liquid

  • NDC Code(s): 27426-020-10, 27426-020-50
  • Packager: Penleigh Irving Ltd
  • 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 January 2, 2019

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

  • SAFE HANDLING WARNING

    Keep away from children. Flammable liquid and vapour. Keep away from heat/sparks/open flames/hot surfaces. No smoking. Harmful in contact with skin. Causes skin irriation. May cause an allergic skin reaction. Harmful if inhaled. Keep container tightly closed. May be fatal if swallowed and enters airways. If swallowed: immediately call a poison centre or doctor. Do not induce vomiting. May cause drowsiness or dizziness. Causes damage to organs through prolonged or repeated exposure. Avoid breathing vapour/spray. Do not get in eyes, or skin or on clothing. Store locked up. Use only outdoors or in a well-ventilated area. If on skin: Wash with plenty of soap and water. If skin irritation or rash occurs: Get medical advice/attention. If in eyes: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing until no signs of contamination remain. Harmful/toxic to acquatic life with long lasting effects. Avoid release to the environment. Dispose of contents/container in accordance with local regulation. Causes serious eye irritation. Do not breath vapor. Wear protective gloves/protective clothing/eye protection/face protection.

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  • PRINCIPAL DISPLAY PANEL

    Keratex Hoof Gel

    Helps prevent hooves from softening in wet, muddy conditions. Regular use will assist the horse in fighting the effects of everyday life on hooves, such as climate, stabling, schooling and roadwork.

    Shake Before Use. Start with a clean, dry hoof. After several applications the hoof will be easier to clean and dry as most water will run off, and what remains can be dried with a cloth. Apply to the hoof wall using a hoof brush. Start just below the coronary band and work downwards. For complete protection, apply to the sole and frog as well. Allow to dry before riding or turning out. When dry, buff with a cloth for a natural sheen.

    Keratex Hoof Gel preserves moisture within the hoof at the optimum level. This maintains the flexibility of the hoof wall, heel, sole and frog of the horse’s feet.

    Do not use conventional hoof oils and greases with Keratex Hoof Gel. Use every 2 days except in dry conditions, when Hoof Gel can be applied every 4 days. Apply an extra coat before riding out in snow or in extremely wet, muddy conditions.

    For External Use on Hooves Only.

    Keep away from horse's eyes, nose and mouth. Not to be used on animals intended for human consumption.

    Hoof Gel Ingredients Statement. This product contains: Stoddard Solvent (White Spirit) CAS 8052-41-3. Turpentine CAS 8006-64-2. Aluminium Stearate CAS 637-12-7.

    33.81 fl oz (1 Litre)

    Made in UK

    Penleigh Irving Ltd.

    Dilton Marsh, Wiltshire, BK13 3SN, UK

    +44 (0) 1373 827649 email: info@keratex.com

    www.keratex.com

    KHG 1000

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  • INGREDIENTS AND APPEARANCE
    KERATEX  KHG
    aluminum stearate liquid
    Product Information
    Product Type OTC ANIMAL DRUG Item Code (Source) NDC:27426-020
    Route of Administration Topical
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALUMINUM STEARATE (UNII: U6XF9NP8HM) (ALUMINUM STEARATE - UNII:U6XF9NP8HM) ALUMINUM STEARATE 2.5 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    TURPENTINE (UNII: XJ6RUH0O4G)  
    WHITE SPIRIT TYPE 1 (UNII: 37LNJ1I16R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:27426-020-50 500 mL in 1 BOTTLE
    2 NDC:27426-020-10 1000 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 08/01/1999
    Labeler - Penleigh Irving Ltd (505992479)
    Establishment
    Name Address ID/FEI Business Operations
    Penleigh Irving Ltd 505992479 api manufacture, manufacture
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