Label: MOLLENOL- eugenia caryophylata, santalum spicatum ointment

  • 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 October 15, 2018

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

View All Sections
  • ACTIVE INGREDIENT

    Eugenia caryophylata 60% w/w

    Santalum Spicatum 0.2% w/w

  • INACTIVE INGREDIENT

    Coconut Oil

  • INDICATIONS & USAGE

    MCV relief

    Molluscum contagiosum lesion relief.

  • PURPOSE

    MCV Relief

  • DOSAGE & ADMINISTRATION

    Apply 2 times daily directly to each molluscum

    Do not rub in.

    Cover with bandage if possible.

  • WARNINGS

    For external use only.

    Keep out of reach of children.

    Do not use on wounds, punctured skin or near or in eyes.

    Stop use and ask doctor if rash or allergic reaction occurs or condition worsens.

    If swallowed induce vomit, seek medical help, or contact a Poison Control Center right away.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.​

  • PRINCIPAL DISPLAY PANEL

    Mollenol

  • INGREDIENTS AND APPEARANCE
    MOLLENOL 
    eugenia caryophylata, santalum spicatum ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72269-019
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLOVE (UNII: K48IKT5321) (CLOVE - UNII:K48IKT5321) CLOVE60 mg  in 100 mL
    SANTALUM SPICATUM WHOLE (UNII: O8PUT104O1) (SANTALUM SPICATUM WHOLE - UNII:O8PUT104O1) SANTALUM SPICATUM WHOLE0.2 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    COCONUT OIL (UNII: Q9L0O73W7L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72269-019-0125 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic10/15/2018
    Labeler - Jeva Laboratories (751297250)
    Registrant - Jeva Laboratories (751297250)
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!