Label: 7.5% HYPERTONIC SALINE- hypertonic saline solution liquid

  • NDC Code(s): 50480-124-99
  • Packager: Radix Laboratories, 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 December 22, 2014

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  • • CONTENTS (grams/100ml):

    • Sodium Chloride .....7.5
  • Inactives:

    • Purified Water  q.s.
    • Methylparaben
    • Propylparaben
    • Citric Acid
  • Indications:

    • For use as a supplemental nutritive source of sodium chloride in cattle.
  • Storage:

    • Store at controlled room temperature between 59oF to 86oF (15oC -30oC).
  • Warnings:

    • Avoid storage at cold temperatures which can cause product to become cloudy.
    • To clarify place product in warm water bath (100oF-120oF) for about 30 minutes.
  • Dosage and administration:

    • Administer orally as a drench or by use of a stomach tube.
    • The usual recommended dose in adult cattle is 16.9 fl. oz (500mL) to 33.8 fl.oz (1000mL) depending on size and condition.
  • KEEP OUT OF REACH OF CHILDREN

    • Keep away from children.
  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel

    Item image

    7.5% NaCl 1000ml

  • INGREDIENTS AND APPEARANCE
    7.5% HYPERTONIC SALINE 
    hypertonic saline solution liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:50480-124
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE7.5 g  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50480-124-9912 in 1 CARTON
    11000 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/27/2013
    Labeler - Radix Laboratories, Inc. (108500091)