HEX-PLUS- teat dip liquid

Hex-PLUS by

Drug Labeling and Warnings

Hex-PLUS by is a Animal medication manufactured, distributed, or labeled by Tetradyne LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

USE DIRECTIONS:
Use at full strength, do not dilute.

POST-MILKING:

Dip entire teat in HEX-PLUS.  Allow to air dry.
If solution in cup becomes visibly dirty.  Then
replenish with HEX-PLUS at full strength.  Do
not return unused product to original container.


PROTECT FROM FREEZING
IF FROZEN: SHAKE VIGOROUSLY
AFTER THAWING

WARNINGS AND PRECAUTIONS

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.

PRINCIPAL DISPLAY PANEL

HEX-PLUS

SANITIZING CHLORHEXIDINE TEAT DIP
FORMULATED WITH EMOLLIENTS AND
DERMAL CONDITIONERS

This product, when properly used, is effective as an aid
in reducing the spread of organisms which may cause
mastitis.

Active Ingredient..........1.0% Chlorhexidine Gluconate

Contains 10% Emollient

Lot#:______________________

Exp. Date:___________________

Next Content:________________

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

INGREDIENTS AND APPEARANCE

HEX-PLUS 
teat dip liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 66399-742
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	1.0 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	10 L  in 100 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66399-742-01	3.78 L in 1 JUG
2	NDC: 66399-742-02	18.9 L in 1 PAIL
3	NDC: 66399-742-03	56.7 L in 1 DRUM
4	NDC: 66399-742-04	113.4 L in 1 DRUM
5	NDC: 66399-742-05	207.9 L in 1 DRUM
6	NDC: 66399-742-06	945 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
7	NDC: 66399-742-07	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)