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Hex-Wash

Generic name: chlorhexidine gluconate liquid
Dosage form: FOR ANIMAL USE ONLY

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA.

USE DIRECTIONS:

Do not use in concentrated form. Must
be diluted prior to use.


DILUTIONS:

Pre-mix one (1) ounce Hex-Wash with five (5)
gallons of water. Use a separate towel for each
cow and discard towel after applications, then rinse
with warm water and examine each quarter with
strip cup.


PROTECT FROM FREEZING
IF FROZEN: SHAKE VIGOROUSLY
AFTER THAWING

WARNING: CONTAINS CHLORHEXIDINE
GLUCONATE.

Not for human use.
Avoid contamination of food. Avoid contact
with eyes. Not for internal use.


OBSERVE LABEL DIRECTIONS

KEEP OUT OF REACH OF CHILDREN!

FIRST AID:
INTERNAL:
If swallowed, do not induce vomiting.
Drink large quantities of water. See physician immediately.

EYES: Flush eyes with clear water for 15 minutes.If irritated, obtain medical guidance.


GET MEDICAL ATTENTION IMMEDIATELY.

Hex-Wash

CHLORHEXIDINE GLUCONATE UDDER WASH


Active Ingredient.....0.50% Chlorhexidine Gluconate


Lot#:______________________

Exp. Date:___________________

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Manufactured For:
Tetradyne LLC
PO Box 17003
Reno, NV 89511

Hex-Wash
Hex-Wash liquid
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:66399-738
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE) CHLORHEXIDINE GLUCONATE 0.5 L in 100 L
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
Packaging
# Item Code Package Description
1 NDC:66399-738-01 3.78 L in 1 JUG
2 NDC:66399-738-02 18.9 L in 1 PAIL
3 NDC:66399-738-03 56.7 L in 1 DRUM
4 NDC:66399-738-04 113.4 L in 1 DRUM
5 NDC:66399-738-05 207.9 L in 1 DRUM
6 NDC:66399-738-06 945 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
7 NDC:66399-738-07 1039.5 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 09/10/2001
Labeler - Tetradyne LLC (130969293)
Tetradyne LLC