Label: KETO-PLEX FORTE liquid
- NDC Code(s): 50480-010-99
- Packager: Radix Laboratories, Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 22, 2014
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- Official Label (Printer Friendly)
- CONTENTS (Per 1000ml):
- Inactives:
- Indications:
- Storage:
- Warnings:
- Dosage and administration:
- Keep Away From Children
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
KETO-PLEX FORTE
keto-plex forte liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50480-010 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CHLORIDE 0.330 g in 1000 mL MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CHLORIDE 0.260 g in 1000 mL AMINO ACIDS (UNII: 0O72R8RF8A) (AMINO ACIDS - UNII:0O72R8RF8A) AMINO ACIDS 2.7 g in 1000 mL DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 300 g in 1000 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50480-010-99 12 in 1 CARTON 1 1000 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/27/2013 Labeler - Radix Laboratories, Inc. (108500091)