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 100 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:52533-171
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)

Revised: 5/2014
Document Id: 0876071f-9b42-4799-8f16-fda80c5b7306
Set id: 20562220-5425-4eb4-9b52-52851f8c9977
Version: 8
Effective Time: 20140527
 
Cantrell Drug Company