Label: GUNA-TF PAPILLOMA- human papillomavirus capsule, gelatin coated

  • Category: HUMAN OTC DRUG LABEL

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 March 31, 2010

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENTS/PURPOSE

    TRANSFER FACTOR HPV    7X    STIMULATES DEFENSIVE AND RECOVER FROM PAPILLOMA INFECTIONS

  • USES


    For the temporary relief of symptoms due to Papilloma infections such as: itching, burning, minor discomfort


  • WARNINGS

    Stop use and ask doctor if symptoms of itching or minor discomfort worsen or persist more than 5 days

  • PREGNANCY

    If pregnant or breast-feeding ask a doctor before use

  • WARNINGS

    Keep this and all medicines out of reach of children

  • DIRECTIONS

    Take 15 minutes before meals
    Adults 18 years and older    1 capsule per day with a little water

  • QUESTIONS

    Questions?: info@gunainc.com
    Tel. (484) 223-3500

  • PRINCIPAL DISPLAY PANEL

    image of box label

  • INGREDIENTS AND APPEARANCE
    GUNA-TF PAPILLOMA 
    human papillomavirus capsule, gelatin coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17089-281
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J) (HUMAN PAPILLOMAVIRUS - UNII:23CVL7WF4J) HUMAN PAPILLOMAVIRUS7 [hp_X]  in 4600 mg
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G) 4048 mg  in 4600 mg
    MAGNESIUM STEARATE (UNII: 70097M6I30) 92 mg  in 4600 mg
    Product Characteristics
    Colorwhite (white) Score2 pieces
    ShapeOVAL (Capsule) Size18mm
    FlavorImprint Code na
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17089-281-101 in 1 BOX
    14600 mg in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/16/2008
    Labeler - Guna spa (430538264)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guna spa430538264manufacture
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

More Info on this Drug

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