Label: LUMICAIN- aluminium chloride hexahydrate solution

  • NDC Code(s): 10733-412-60
  • Packager: Medical Products Laboratories, Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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.

Drug Label Information

Updated December 23, 2020

If you are a consumer or patient please visit this version.

View All Sections
  • DOSAGE & ADMINISTRATION

    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.

  • WARNINGS AND PRECAUTIONS

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

  • PRINCIPAL DISPLAY PANEL

    lblpremier lumicain TM Topical Hemostatic Solution 60cc

    For Rapid Control of Minor Hemorrhage

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

    In an aqueous base.

    Enter section text here

  • INGREDIENTS AND APPEARANCE
    LUMICAIN 
    aluminium chloride hexahydrate solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:10733-412
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE250 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10733-412-6067 g in 1 BOTTLE; Type 0: Not a Combination Product09/29/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/29/2010
    Labeler - Medical Products Laboratories, Inc. (002290302)
    Registrant - Medical Products Laboratories, Inc. (002290302)
    Establishment
    NameAddressID/FEIBusiness Operations
    Medical Products Laboratories, Inc.002290302analysis(10733-412) , manufacture(10733-412) , label(10733-412) , pack(10733-412)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!