PRO-PRIN- sodium salicylate granule

Pro-Prin by

Drug Labeling and Warnings

Pro-Prin by is a Animal medication manufactured, distributed, or labeled by AHC Products Inc, Universal Preserv-A-Chem. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS AND PRECAUTIONS

CAUTION:

THIS PRODUCT IS DESINGED FOR USE IN SWINE AND POULTRY ONLY.

WARNINGS:

DO NOT USE IN PIGLETS LESS THAN 3 WEEKS OF AGE

NOT FOR HUMAN USE

KEEP OUT OF THE REACH OF CHILDREN 

INDICATIONS & USAGE

Pro-Prin is designed to provide Sodium Salicylate through the animals drinking water. 

DOSAGE & ADMINISTRATION

To reconstitute add 1 scoop (approximately 20 ounces) to 5 gallons of water to make stock solution. Meter 1:128 (1 fluid ounce per gallon) of drinking water. Prepare fresh stock solution daily. Repeat as needed.

WATER PROPORTIONER USE: Add 20 ounces (1 scoop) of Pro-Prin to make 5 gallons of stock solution and administer through a medicator metered at 1:128 (1 ounce per gallon). THis will achieve a target does of 22.7 mg/lb (50 mg/kg) body weight daily.

FOR ANTI-INFLAMMATORY/ANTI-PROSTAGLANDIN USE - DAY 1

WATER PROPROPORTIONER USE: Add 40 ounces (2 scoops) of Pro-Prin to make 5 gallons of stock solution and administer through a medicator metered at 1:128 (1 ounce per gallon). This will achieve a target does of 22.7 mg/lb (50 mg/kg) body weight daily. 

DAY 2 THROUGH 7

WATER PROPORTIONER USE: Add  25 ounces (1.25 scoop) of Pro-Prin to make 5 gallon of stock solution and administer through a medicator metered at 1:128 (1 ounce per gallon). This will achieve a target dose of 13.6 mg/lb (30 mg/kg) body weight daily. 

ACTIVE INGREDIENT

ACTIVE INGREDIENT:

Sodium Salicylate 100.0% w/v

PRINCIPAL DISPLAY PANEL

CVE

ClearViewEnterprises

Water Soluble Sodium Salicylate

Pro-Prin

5

NDC: 65090-005-46

NET CONTENTS: 16 lbs (7257.48 gms)

For use in poultry and swine

INGREDIENTS AND APPEARANCE

PRO-PRIN 
sodium salicylate granule

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 65090-005
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SODIUM SALICYLATE	28.3 g  in 28.3 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65090-005-46	7257.48 g in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/19/2017

Labeler - AHC Products Inc (169764193)

Establishment
Name	Address	ID/FEI	Business Operations
AHC Products Inc		169764193	manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Universal Preserv-A-Chem		057434664	api manufacture