Label: SKIN TAG SOLUTION- thuja occidentalis liquid

  • 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 June 30, 2015

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  • ACTIVE INGREDIENT

    THUJUS OFFICINALIS 6X

  • PURPOSE

    POLPI, NAEVI, SKIN TUBERCLES SYMPTOMS

  • USES

    SYMPTOMATIC TREATMENT OF SKIN TAGS

  • WARNINGS

    FOR EXTERNAL USE ONLY. AVOID USING NEAR EYES.

    IF PREGNANT OR BREAST FEEDING, ASK A MEDICAL PROFESSIONAL.

  • KEEP OUT OF REACH OF CHILDREN.

  • DIRECTIONS

    • APPLY 3-4 TIMES DAILY TO AFFECTED AREA.
    • SKIN TAGS WILL DRY AND FALL OFF OVER A 4 TO 8 WEEK PERIOD WITH REGULAR USE.
    • IF IRRITATION OCCURS, DISCONTINUE USE.
  • OTHER INFORMATION

    • PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUNLIGHT.
  • PRINCIPAL DISPLAY PANEL

    SKIN TAGE SOLUTION LABEL

  • INACTIVE INGREDIENTS

    BHT, GLYCINE SOYA (SOYBEAN) OIL, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, MELALEUCA ALTERNIFOLIA (TEA TREE) OIL, PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL AND SD-ALCOHOL 40B.

  • INGREDIENTS AND APPEARANCE
    SKIN TAG SOLUTION 
    thuja occidentalis liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69368-2454
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N) (THUJA OCCIDENTALIS WHOLE - UNII:5HBV6WCE3N) THUJA OCCIDENTALIS WHOLE6 [hp_X]  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    ALMOND OIL (UNII: 66YXD4DKO9)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69368-2454-415 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product04/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/01/2015
    Labeler - VITACOST.COM, INC. (949697700)
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