Label: ABSORBINE HOOFLEX THRUSH REMEDY- chloroxylenol and alcloxa liquid
- NDC Code(s): 11444-029-04
- Packager: W. F. Young, Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Updated January 11, 2013
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- VETERINARY INDICATIONS
- Kills Germs on Contact, Not Tissue
- Will Not Dry Out Hooves
- No Spills, Stains or Mess
Hooflex® Thrush Remedy kills embedded bacteria and fungi and helps promote normal healing. Symptoms of thrush include thick black discharge around the frog, accompanied by a foul odor. White Line Disease is an infection that begins at the hoof sole's white line and extends upward into the hoof wall. Cavities form in the hoof wall and emit a foul odor.Close
No shaking necessary.
- After cleaning the hoof, apply Thrush Remedy into clefts of frog and any holes or cracks.
- For active infections, treat once daily for at least three days.
- For maintenance, treat twice weekly.
KEEP OUT OF REACH OF CHILDREN. FOR EXTERNAL USE ONLY ON HORSES OR LIVESTOCK. If condition persists longer than two weeks, call your veterinarian. Avoid contact with eyes. In case of contact, immediately flush eye with plenty of water.Close
- Active Ingredients
Chloroxylenol 5.0%; Alcloxa 0.25%Close
- Inactive Ingredients
Propylene glycol, Terpineol, WaterClose
- SPL UNCLASSIFIED SECTION
W. F. Young, Inc.
302 Benton Drive
East Longmeadow, MA 01028
- PRINCIPAL DISPLAY PANEL - 355 mL Bottle Label
BACTERICIDAL + FUNGICIDAL
Helps Promote Healthy Tissue
Kills and Prevents Bacteria
No Sting, No Stain
12 fl oz (355 ml)
- INGREDIENTS AND APPEARANCE
ABSORBINE HOOFLEX THRUSH REMEDY
chloroxylenol and alcloxa liquid
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:11444-029 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q) Chloroxylenol 5 g in 100 mL Alcloxa (UNII: 18B8O9DQA2) (Alcloxa - UNII:18B8O9DQA2) Alcloxa 0.25 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Propylene Glycol (UNII: 6DC9Q167V3) Terpineol (UNII: R53Q4ZWC99) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11444-029-04 355 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 01/01/1974 Labeler - W. F. Young, Inc. (001114669)