Label: 1% ALOE VERA TD- iodine solution

  • NDC Code(s): 86067-0110-1, 86067-0110-2, 86067-0110-3, 86067-0110-4, view more
    86067-0110-5
  • Packager: Surpass Chemical 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 6, 2023

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

View All Sections
  • DESCRIPTION

    NORTH COUNTRY DAIRY SUPPLY, LLC.                                                       PRODUCT #: 631150                              NPE

    Metz 1% Aloe Vera Teat Dip                                                                                                                                           FREE

    An aid in a complete cow care program to help control external organisms that may cause mastitis.

  • INSTRUCTIONS FOR USE

    DIRECTIONS:
    Before milking, dip or spray the entire teat with this product. Wipe teats dry after application using a single service towel to avoid milk contamination. Immediately after milking, submerge entire teat up to the base of the udder in an UNDILUTED solution of NCDS METZ 1% ALOE VERA TEAT DIP. Allow to air dry. Do not wipe.

  • GENERAL PRECAUTIONS

    CAUTION:
    Only use as directed. Do not take internally. Avoid contact with eyes, skin, clothing, and food. Avoid breathing vapors. Always use full strength Teat Dip. Discard solution if it becomes faded or noticeably dirty. Do not use this dip to sanitize milking equipment or utensils.

  • ACTIVE INGREDIENT

    INGREDIENTS:
    ACTIVE: Iodine complex (Provides 0.75% titratable iodine. Equivalent to 7,500 ppm).

  • OTHER SAFETY INFORMATION

    FIRST AID:
    IF SPLASHED IN EYES: Rinse immediately with plenty of water, also under the eyelids, for at least 15 minutes. Get medical attention if irritation occurs.
    IN CASE OF CONTACT: Wash off immediately with plenty of water for at least 15 minutes. Get medical attention if symptoms occur.
    IF INHALED: Move to fresh air. If symptoms persist, call a physician.
    IF SWALLOWED: Drink plenty of water. Do NOT induce vomiting. Never give anything by mouth to an unconscious person. Consult a physician if necessary

  • SAFE HANDLING WARNING

    BEFORE USING THIS MATERIAL, READ AND
    UNDERSTAND THE CURRENT SAFETY DATA SHEET.

  • SPL UNCLASSIFIED SECTION

    Surpass Chemical Company, Inc.                                                                                           24 HOUR EMERGENCY ASSISTANCE:
    www.surpasschemical.com               Phone: (518) 434-8101                                                           CHEMTREC 1-800-424-9300
    1254 Broadway                                 Fax: (518) 434-2798

    Albany NY, 12204                               Email: customerservice@surpasschemical.com

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN!

  • SPL UNCLASSIFIED SECTION

    NOT A DOT
    HAZARDOUS MATERIAL

  • PRINCIPAL DISPLAY PANEL


    image description

  • INGREDIENTS AND APPEARANCE
    1% ALOE VERA TD 
    iodine solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:86067-0110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE0.0476 kg  in 1 kg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) .7796 kg  in 1 kg
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.049 kg  in 1 kg
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.005 kg  in 1 kg
    C9-11 PARETH-3 (UNII: 8O4974OMUO) 0.0605 kg  in 1 kg
    GLYCERIN (UNII: PDC6A3C0OX) 0.0954 kg  in 1 kg
    SODIUM HYDROXIDE (UNII: 55X04QC32I) 0.008 kg  in 1 kg
    XANTHAN GUM (UNII: TTV12P4NEE) 0.0008 kg  in 1 kg
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA) 0.0016 kg  in 1 kg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:86067-0110-24 in 1 BOX
    1NDC:86067-0110-13.97 kg in 1 JUG
    2NDC:86067-0110-359.87 kg in 1 DRUM
    3NDC:86067-0110-4218.63 kg in 1 DRUM
    4NDC:86067-0110-5992.23 kg in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/06/2023
    Labeler - Surpass Chemical Company, Inc. (002075133)
    Establishment
    NameAddressID/FEIBusiness Operations
    Surpass Chemical Company, Inc.002075133manufacture, api manufacture
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events (Animal Drug), FDA Safety Recalls (Animal Drug)

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!