KAO-PECT PLUS- kaolin pectin suspension

KAO-PECT by

Drug Labeling and Warnings

KAO-PECT by is a Animal medication manufactured, distributed, or labeled by PHOENIX PHARMACEUTICAL INC./ CLIPPER DISTRIBUTING, INC., FIRST PRIORITY INCORPORATED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

ANTI-DIARRHEAL LIQUID

KEEP OUT OF REACH OF CHILDREN

FOR ANIMAL USE ONLY
KEEP OUT OF REACH OF CHILDREN

INDICATIONS:

For oral administration as an aid in the treatment of noninfectious diarrhea in horses, cattle, dogs and cats.

DIRECTIONS FOR USE:

Administer orally after first sign of diarrhea and after each loose bowel movement, or as needed.

Cattle and Horses – 6 to 10 fl oz
Calves and Foals – 3 to 4 fl oz
Dogs and Cats – 1 to 3 tablespoonfuls

CAUTION:

If symptoms persist after using this product for 2-3 days, consult a veterinarian.

ACTIVE INGREDIENTS:

Each fluid ounce (2 tablespoonfuls) contains:
Kaolin ........................................ 90 gr. (5.8 g)
Pectin ...................................... 4 gr. (0.268 g)

INACTIVE INGREDIENTS:

Purified Water, Xanthan Gum, Artificial Flavors, Methyl Paraben, Artificial Color, Propyl Paraben, Sodium Saccharin.

STORAGE:

Store at controlled room temperature between 15°-30°C (59°-86°F). Keep container tightly closed when not in use.
Protect from freezing.
SHAKE WELL BEFORE USING.

Net Contents:

One Gallon (3.785 L)

INFORMATION FOR OWNERS/CAREGIVERS

Trademarks are property of Clipper Distributing Company, LLC

Manufactured by:
First Priority, Inc.
Elgin, IL U.S.A.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KAO-PECT  PLUS
kaolin pectin suspension

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 57319-606
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KAOLIN (UNII: 24H4NWX5CO) (KAOLIN - UNII:24H4NWX5CO)	KAOLIN	208.1 g  in 1 L

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY, VANILLA	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57319-606-09	4 in 1 CASE
1		3.785 L in 1 JUG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/14/2018

Labeler - PHOENIX PHARMACEUTICAL INC./ CLIPPER DISTRIBUTING, INC. (150711039)

Establishment
Name	Address	ID/FEI	Business Operations
FIRST PRIORITY INCORPORATED		179925722	api manufacture, manufacture, label