AQUASOURCE LIQUID SODIUM SALICYLATE PLUS CAFFEINE- sodium salicylate liquid

AquaSource Liquid Sodium Salicylate plus Caffeine by

Drug Labeling and Warnings

AquaSource Liquid Sodium Salicylate plus Caffeine by is a Animal medication manufactured, distributed, or labeled by Blendpack, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS

For use in the drinking water of poultry and swine as an aid in reducing pain, fever and inflammation

WARNINGS

Not for use in lactating dairy cattle.

A withdrawal period of 24 hours is recommended in meat.

Not for human use.

Keep container tightly closed.

Keep out of reach of children.

Store at room temperature.

ACTIVE INGREDIENTS

Sodium Salicylate - 120,000 milligrams/liter (3,548 mg per oz.)
Caffeine - 1.14% w/v

CONTENTS

White willow (Salix alba bark extract), disodium phosphate, monopotassium phosphate, and water

DIRECTIONS FOR USE

Mix the following amounts of Liquid Sodium Salicylate into the drinking water daily as analgesic/antipyretic or anti-inflammatory for:

Growing swine - ages wean to market

Growing chickens - ages 0-15 weeks

Growing turkeys - ages 0-24 weeks

Analgesic and Antipyretic: 

Mix 3 ounces of Liquid Sodium Salicylate per 1000 lb bodyweight (210 mL per 1000 kg) into the drinking water daily to provide the target dose of 25 mg sodium salicylate per kg bodyweight. 

Anti-Inflammatory / Anti-prostaglandin Effect:

First Day - Mix 6 ounces of Liquid Sodium Salicylate per 1000 lb bodyweight (420 mL per 1000 kg) into the drinking water daily to provide the target dose of 50 mg sodium salicylate per kg bodyweight. 

Following Days - Mix 3.5 ounces of Liquid Sodium Salicylate into the drinking water daily to provide the target dose of 30 mg sodium salicylate per kg bodyweight. 

Prepare fresh solutions daily. Repeat as necessary. 

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

AQUASOURCE LIQUID SODIUM SALICYLATE PLUS CAFFEINE 
sodium salicylate liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 86050-3120
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SODIUM SALICYLATE	120 g  in 1 L
CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E)	CAFFEINE	11.4 g  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86050-3120-1	.95 L in 1 JUG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/30/2024

Labeler - Blendpack, Inc. (043362034)

Establishment
Name	Address	ID/FEI	Business Operations
Blendpack, Inc.		043362034	manufacture