Label: PRO-PRIN- sodium salicylate granule
- NDC Code(s): 65090-005-46
- Packager: AHC Products Inc
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated June 18, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- WARNINGS AND PRECAUTIONS
- INDICATIONS & USAGE
-
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
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
PRO-PRIN
sodium salicylate granuleProduct 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
