AquaPrime Liquid Sodium Salicylate

AquaPrime Liquid Sodium Salicylate by

Drug Labeling and Warnings

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

Drug Details [pdf]

AQUAPRIME LIQUID SODIUM SALICYLATE- sodium salicylate liquid 
Blendpack, Inc.

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.

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AquaPrime Liquid Sodium Salicylate

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.

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 0.6 ounces of Liquid Sodium Salicylate per 1000 lb bodyweight (42 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 1.2 ounces of Liquid Sodium Salicylate per 1000 lb bodyweight (84 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 0.7 ounce of Liquid Sodium Salicylate per 1000 lb bodyweight (50 mL per 1000 kg) 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.

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AQUAPRIME LIQUID SODIUM SALICYLATE 
sodium salicylate liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 86050-2600
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SODIUM SALICYLATE	600 g  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86050-2600-1	3.79 L in 1 JUG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/27/2023	11/05/2024

Labeler - Blendpack, Inc. (043362034)

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

Revised: 11/2024

Document Id: 78f05dc0-adcb-48b3-b4a4-032e5fd53b7b

50577-6

Set id: bba339ca-8d3e-4ad8-ac42-318a6a801031

Version: 3

Effective Time: 20241105