TETRA KOTE- 0.2% bronopol teat dip solution

Tetra Kote by

Drug Labeling and Warnings

Tetra Kote by is a Animal medication manufactured, distributed, or labeled by Preserve International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DIRECTIONS FOR USE:

Use at full strength, do not dilute.

APPLICATION:

FOR POST-DIPPING:  Immediately after removal of milking unit, dip entire teat in TETRA KOTE.  Allow to air dry.  If solution in cup becomes visibly dirty or cloudy, then replenish with TETRA KOTE at full strength.  Do not return unused product to original container.

NOTE:

This product does not contain NPE (Nonylphenol Ethoxylate) Surfactant.

PROTECT FROM FREEZING

IF FROZEN:  SHAKE VIGOROUSLY AFTER THAWING

TAKE TIME  OBSERVE LABEL DIRECTIONS

WARNING:

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

KEEP OUT OF REACH OF CHILDREN

FIRST AID:

INHALATION: No irritation expected.  Move the exposed person to fresh air.

EYE ​CONTACT​:​  Rinse immediately with plenty of water.  Contact lenses should be removed.

​SKIN CONTACT:​  No irritation expected.  Rinse immediately with plenty of water. 

​INGESTION:​  DO NOT INDUCE VOMITING unless advised to do so by a doctor.  Never give anything by mouth to an unconscious person.

GET MEDICAL ATTENTION IMMEDIATELY.

​FOR PRODUCT EMERGENCY CONTACT:  Chem-Tel Inc. 1-800-255-3924

PRINCIPAL DISPLAY PANEL

TETRA kOTE

Barrier Post Dip

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

Active Ingredient..........0.20% 2-Bromo-2-Nitro 1,3 propanediol
pH.....................................Minimum 4.0
Emollients........................10% Glycerin

Manufactured By: Preserve International​®​

Preserve International​®​ is a wholly-owned subsidiary of Neogen​®​ Corporation.

NEOGEN​®​

944 Nandino Blvd.

Lexington, KY  40511

859-254-1221 or 800-621-8829

animalsafety.neogen.com

INGREDIENTS AND APPEARANCE

TETRA KOTE 
0.2% bronopol teat dip solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 60648-9008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BRONOPOL (UNII: 6PU1E16C9W) (BRONOPOL - UNII:6PU1E16C9W)	BRONOPOL	2.16 g  in 1 L
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	104.20 g  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60648-9008-1	3.78 L in 1 JUG
2	NDC: 60648-9008-2	18.9 L in 1 PAIL
3	NDC: 60648-9008-3	56.7 L in 1 DRUM
4	NDC: 60648-9008-4	113.4 L in 1 DRUM
5	NDC: 60648-9008-5	207.9 L in 1 DRUM
6	NDC: 60648-9008-6	945 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
7	NDC: 60648-9008-7	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		03/18/2019

Labeler - Preserve International (808154199)