Label: HEXI-DIP 1%- chlorhexidine gluconate liquid

  • NDC Code(s): 63927-4185-1, 63927-4185-2, 63927-4185-3, 63927-4185-4, view more
    63927-4185-5
  • Packager: ProActive Solutions USA, LLC
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated December 19, 2023

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  • Hexi-Dip 1%

    Hexi-Dip 1%™ is a post-milking sanitizing teat dip to aid in the prevention of the spread of
    mastitis causing organisms. It’s powerful 1.0% Chlorhexidine Gluconate concentration
    assures strong germicidal activity while ample amounts of special skin emollients
    keep teats soft and smooth.

    Use instructions:

    Immediately after removing inflations, immerse each teat in undiluted
    Hexi-Dip 1%™.

    Allow the teats to air dry. Do not wipe.

    Replace the solution if it becomes visibly dirty.

    Keep from freezing. If frozen, thaw completely and shake well before using.

    Caution:

    Hazard statement(s)                                                                                                                                                                                     May be harmful if swallowed. May cause eye irritation.
    Precautionary statement(s):
    Do not eat, drink or smoke while using this product. Wear protective clothing, and eye
    and face protection.
    Hazards not otherwise classified: None Known

    First Aid:

    External: If irritation occurs, flush with plenty of cool, running water for at least 15                                                                                minutes while removing contaminated clothing and shoes. Wash clothing before
    reuse.
    Eyes: Immediately flush with plenty of cool, running water. Remove contact lenses;
    then continue flushing for at least 15 minutes, holding eyelids apart.
    Internal: Call a physician immediately. If swallowed, do not induce vomiting. Rinse
    mouth, then immediately drink one or two large glasses of water or milk. Never give
    anything by mouth to an unconscious person.
    Inhalation of vapors: Should not occur with proper use of this product.
    Most important symptoms/effects, acute and delayed: None known
    Immediate medical attention and special treatment needed, if any: None known

  • Hexi-Dip 1%

    Hexi-Dip 1
  • INGREDIENTS AND APPEARANCE
    HEXI-DIP 1% 
    chlorhexidine gluconate liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:63927-4185
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE1 kg  in 100 kg
    Inactive Ingredients
    Ingredient NameStrength
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD) 0.0136 kg  in 100 kg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63927-4185-115.28 kg in 1 DRUM
    2NDC:63927-4185-219.11 kg in 1 DRUM
    3NDC:63927-4185-357.31 kg in 1 DRUM
    4NDC:63927-4185-4114.62 kg in 1 DRUM
    5NDC:63927-4185-5210.14 kg in 1 DRUM
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/30/2009
    Labeler - ProActive Solutions USA, LLC (029368225)
    Registrant - ProActive Solutions USA, LLC (029368225)
    Establishment
    NameAddressID/FEIBusiness Operations
    ProActive Solutions USA, LLC029368225api manufacture, manufacture, pack, repack, label