Label: PHENYLEPHRINE HCL - phenylephrine hydrochloride injection, solution

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

Drug Label Information

Updated 05/14

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  • INGREDIENTS AND APPEARANCE
    PHENYLEPHRINE HCL 
    phenylephrine hcl injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-171
    Route of Administration INTRAVENOUS DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV) Phenylephrine Hydrochloride 100 ug  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Sodium Chloride (UNII: 451W47IQ8X) 9 mg  in 1 mL
    Water (UNII: 059QF0KO0R)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C) 0.2 mg  in 1 mL
    SODIUM CITRATE (UNII: 1Q73Q2JULR) 0.4 mg  in 1 mL
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.09 mg  in 1 mL
    Other Ingredients
    Ingredient Kind Ingredient Name Quantity
    May contain SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52533-171-12 10 mL in 1 SYRINGE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 08/30/2012
    Labeler - Cantrell Drug Company (035545763)
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