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

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.