Hex-PLUS: Product Information

HEX-PLUS — chlorhexidine gluconate liquid
Tetradyne LLC

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.

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

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-PLUS

SANITIZING CHLORHEXIDINE TEAT DIP
FORMULATED WITH EMOLLIENTS AND
DERMAL CONDITIONERS


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 17003Reno, NV 89511

Package Label
(click image for full-size original)
HEX-PLUS teat dip liquid
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:66399-742
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE) CHLORHEXIDINE GLUCONATE 1.0 L in 100 L
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 10 L in 100 L
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:66399-742-01 3.78 L in 1 JUG None
2 NDC:66399-742-02 18.9 L in 1 PAIL None
3 NDC:66399-742-03 56.7 L in 1 DRUM None
4 NDC:66399-742-04 113.4 L in 1 DRUM None
5 NDC:66399-742-05 207.9 L in 1 DRUM None
6 NDC:66399-742-06 945 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK None
7 NDC:66399-742-07 1039.5 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK None
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)

Revised: 11/2010 Tetradyne LLC

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