PHENYLEPHRINE HCL - phenylephrine hydrochloride injection, solution 
Cantrell Drug Company

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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Phenylephrine HCl 80 mcg/mL in 0.9% Sodium Chloride 10 mL Syringe

Label

PHENYLEPHRINE HCL 
phenylephrine hcl injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-060
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 0.08 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
Sodium Chloride (UNII: 451W47IQ8X) 9 mg  in 1 mL
Water (UNII: 059QF0KO0R)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C) 0.016 mg  in 1 mL
SODIUM CITRATE (UNII: 1Q73Q2JULR) 0.032 mg  in 1 mL
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.072 ug  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:52533-060-12 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)

Revised: 12/2014
Document Id: fa79684a-ba44-4eef-8e88-a892db2aa76a
Set id: 5bda9fa0-f753-4f21-8321-efea39106852
Version: 9
Effective Time: 20141211
 
Cantrell Drug Company