Label: AQUAPRIME LIQUID SODIUM SALICYLATE- sodium salicylate liquid

  • 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 July 28, 2023

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  • 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.

  • PRINCIPAL DISPLAY PANEL

    BRE_AquaPrime_Sodium_Salicylate_60_1_Gal

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  • INGREDIENTS AND APPEARANCE
    AQUAPRIME LIQUID SODIUM SALICYLATE 
    sodium salicylate liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:86050-2600
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ) SODIUM SALICYLATE600 g  in 1 L
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:86050-2600-13.79 L in 1 JUG
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/27/2023
    Labeler - Blendpack, Inc. (043362034)
    Establishment
    NameAddressID/FEIBusiness Operations
    Blendpack, Inc.043362034manufacture