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Lumicain

Generic Name: aluminium chloride hexahydrate
Dosage Form: topical solution

Medically reviewed by Drugs.com. Last updated on Dec 1, 2020.

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.

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 Lumicain TM 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 CATION) 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(10733-412), manufacture(10733-412), label(10733-412), pack(10733-412)
Medical Products Laboratories, Inc.

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