Medic Booster Barrier description, usages, side effects, indications, overdosage, supplying and lots more!

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Medic Booster Barrier

Animal Medic Incorporated

Medic Booster Barrier


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Medic Booster Barrier

ANIMAL MEDIC
Medic Booster® Barrier
Sanitizing Teat Dip

Medic Booster® Barrier Sanitizing Teat Dip is an aid in the prevention of organisms which may cause mastitis.

INGREDIENTS:
Active Ingredient -
2 Bromo
2 Nitro-propandoil ................................................................. 0.20%
Also contains:
Lanolin and proplylene glycol.

KEEP OUT OF REACH OF CHILDREN

CAUTION
CAN CAUSE EYE DAMAGE
PROTECT EYES WHEN HANDLING
DO NOT GET IN EYES OR ON CLOTHING
NOT FOR INTERNAL USE
HARMFUL  IF SWALLOWED
AVOID CONTAMINATION OF FOOD

FIRST AID

IF IN EYES:
In case of contact with eyes, flush immediatley with plenty of water for at least 15 minutes.
Call a physician.

IF SWALLOWED:
DO NOT TAKE INTERNALLY. If swallowed, induce vomiting and call a physician immediately.

CAUTION:  Avoid freezing. If frozen, let thaw and shake thoroughly before using.

FOR MEDICAL INFORMATION IN USA OR CANADA, INFOTRAC (800) 535-5053.

DIRECTIONS FOR USE

Immediately after each cow is milked, dip teats in an undiluted solution of Medic Booster® Barrier Sanitizing Teat Dip. Teats should be dipped to the base of the udder.
At the end of lactation, the teats should be dipped in Medic Booster® Barrier Sanitizing Teat Dip for 4 days after last milking.
Teats and udders should be thoroughly washed* and dried before milking, using potable water and individual towels to prevent contamination of milk, Blot dry.
If the dip becomes visibly dirty or contains sediment, use a fresh solution.

Formula Ingredients contain no Phosphorus.

* Use Animal Medic Cocoas Butter Udder Wash or Animal Medic Green Udder Wash.

Medic Booster Barrier

Teat Dip LIQUID

Product Information

Product Type Otc animal drug label Item Code (Source) NDC:12994-003
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BRONOPOL BRONOPOL 2000 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:12994-003-01 3.78 in 1 JUG
2 NDC:12994-003-02 18.9 in 1 DRUM
3 NDC:12994-003-03 56.7 in 1 DRUM
4 NDC:12994-003-04 113.4 in 1 DRUM
5 NDC:12994-003-05 207.9 in 1 DRUM
6 NDC:12994-003-06 1039.5 in 1 CONTAINER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2005-11-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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