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Hemostatic Solution

Generic Name: aluminum chloride
Dosage Form: solution

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.


Hemostatic Solution is a topical astringent solution of Aluminum Chloride. Gingival retraction can be achieved using a plain gingival retraction cord moistened with Hemostatic Solution.


Discontinue use if irritation appears. For topical application only. Avoid eye contact.


Hemostatic Solution stops gingival bleeding fast. If you should inadvertantly damage the gingival margin during tooth preparation or while placing a strip, band or a cerival matrix, moisten the area with Hemostatic Solution which will control and stop bleeding quickly. Hemostatic Solution contains no epinephrine. The use of vasoconstrictors for gingival retractions and bleeding is potentially dangerous and should be avoided. A plain gingival retraction cord can be dipped in Hemostatic Solution and then placed into the gingival sulcus for its hemostatic action.


For use to aid in cessation of gingival bleeding.


Place 0.5 ml of the hemostatic agent on an absorbent gauze sponge or cotton tip applicator and apply to the bleeding gingival surface under slight pressure for 30 seconds.


Do not use in patients with a known history of hypersensitivity to aluminum chloride.


Federal law restricts this drug to use by or on the order of a licensed dental practitioner.

Hemostatic Solution 
aluminum chloride solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:24794-300
Route of Administration DENTAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Aluminum Chloride (ALUMINUM CATION) Aluminum Chloride 7500 mg  in 30 mL
Inactive Ingredients
Ingredient Name Strength
Propylene Glycol  
Potassium Chloride  
Product Characteristics
Color white (colorless) Score     
Shape Size
Flavor Imprint Code
# Item Code Package Description
1 NDC:24794-300-01 30 mL in 1 JAR
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 01/15/2013
Labeler - Crosstex International Inc. (057728685)
Revised: 10/2014
Crosstex International Inc.