Label: ELROSE LABS- conzerol cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated December 17, 2015

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

  • WARNINGS

    For external use only. do not use on large areas, on wounds, punctured skin, in eyes, animal bites or burns. Stop use if rash or allergic reaction occurs/ condition worsens.

  • ACTIVE INGREDIENT

    SILICEA

    CALCAREA CARBONICA

    THUJA  OIL

    NATRUM MURIATICUM

    KALI BROMATUM

    SULPHAR

    KALI MURIATICUM

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed induce vomit. Get medical help or contact a poison control center right away.

  • PURPOSE

    MCV Relief

  • DOSAGE & ADMINISTRATION

    Clean infected skin area.Apply a small amount(equal to lesion size) on each lesion. Gently rub in circular motion leaving thin cream layer.Repeat treatment 2 to 3 times daily. Let dry for 3 minutes.

  • INDICATIONS & USAGE

    Molluscum Contagiosum Lesion Relief

  • INACTIVE INGREDIENT

    Croton Lechleri
    Emulsifying Wax NF
    Polysorbate 60 
    Magnesium Sulfate 
    Vegetable Glycerine
    Zinc Oxide
    Dimethyl Isosorbide 
    Tea Tree Oil
    Colve Oil
    Wintergreen Oil
    Oragano Oil
    Lemon Balm Oil 
    Cedarwood Oil
    Niaouli Oil
    Eucalyptus Leaf  Oil
    Coconut Oil

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    ELROSE LABS 
    conzerol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70223-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (COLLOIDAL SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE6 mg  in 28.3 mg
    OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE6 mg  in 28.3 mg
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE6 [hp_X]  in 28.3 mg
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION6 mg  in 28.3 mg
    POTASSIUM BROMIDE (UNII: OSD78555ZM) (BROMIDE ION - UNII:952902IX06) POTASSIUM BROMIDE6 mg  in 28.3 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROTON LECHLERI WHOLE (UNII: 9K50DM06OR)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    MAGNESIUM SULFATE (UNII: DE08037SAB)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Zinc Oxide (UNII: SOI2LOH54Z)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    CLOVE OIL (UNII: 578389D6D0)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    OREGANO LEAF OIL (UNII: 7D0CGR40U1)  
    LEMON BALM OIL (UNII: MJ76269K9S)  
    JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)  
    NIAOULI OIL (UNII: D50IC2T8FU)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70223-001-0628.3 mg in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic11/16/2015
    Labeler - Elroselabs Inc. (079977784)
    Establishment
    NameAddressID/FEIBusiness Operations
    Elroselabs Inc.079977784manufacture(70223-001)