Lumicain

Generic Name: aluminium chloride hexahydrate
Dosage Form: topical 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.

Lumicain Topical Hemostatic Solution

FOR TOPICAL APPLICATION ONLY

For Granulation Tissue Growth: Allow packing saturated in Lumicain to remain in nail groove for 48 hours; repeat if necessary.

If hemmorrhage is profuse, dress wound with gauze saturated with Lumicain and allow to remain for 24 hours or longer.

CAUTION: Federal Law restricts sale and use to physician or licensed practitioner.


premier LumicainTM Topical Hemostatic Solution 60cc

For Rapid Control of Minor Hemorrhage

Each Gram Contains: Aluminium Chloride............250 mg.

In an aqueous base.

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Lumicain 
aluminium chloride hexahydrate solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:10733-412
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALUMINUM CHLORIDE (ALUMINUM) ALUMINUM CHLORIDE 250 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
WATER  
Packaging
# Item Code Package Description
1 NDC:10733-412-60 67 g in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 09/29/2010
Labeler - Medical Products Laboratories, Inc. (002290302)
Registrant - Medical Products Laboratories, Inc. (002290302)
Establishment
Name Address ID/FEI Operations
Medical Products Laboratories, Inc. 002290302 analysis, manufacture, label, pack
Revised: 09/2011
 
Medical Products Laboratories, Inc.



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