Label: SINUS-TONE- homeopathic liquid liquid

  • Category: HUMAN PRESCRIPTION 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 February 26, 2014

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

  • Sinus-Tone

    image Sinus-Tone Label

  • ACTIVE INGREDIENT

    Allium cepa 12X; Echinacea 4X; Hydrastis canadensis 4X; Kali bichromicum 12X; Mercurius solubilis 30X; Mercurius sulphuratus ruber 12X; Mucosa nasalis suis 9X, 12X, 6C; Natrum sulphuricum 12X; Nux moschata 6X; Pulsatilla 12X

  • Warnings Section

  • DO NOT USE

    Do not use if neck wrap imprinted "SEALED FOR YOUR PROTECTION" is broken or missing.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • STORAGE AND HANDLING

    Store in cool, dry place out of direct sunlight.

  • QUESTIONS

    Questions? Comments?

    800.990.7085 www.goenergetix.com

  • PURPOSE

    Sinus congestion, sinus pain, hay fever.

  • INACTIVE INGREDIENT

    Purified Water 70%, Glycerin 15%, Ethanol 15%.

  • DOSAGE & ADMINISTRATION

    Take 30 drops orally twice daily or as directed by a healthcare professional. Shake well before use.

  • INDICATIONS & USAGE

    Sinus congestion, sinus pain, hay fever.

  • INGREDIENTS AND APPEARANCE
    SINUS-TONE 
    homeopathic liquid liquid
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:64578-0093
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    onion (UNII: 492225Q21H) (ONION - UNII:492225Q21H) onion12 [hp_X]  in 59.1 mL
    MERCURIC SULFIDE (UNII: ZI0T668SF1) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC SULFIDE12 [hp_X]  in 59.1 mL
    ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA4 [hp_X]  in 59.1 mL
    goldenseal (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) goldenseal4 [hp_X]  in 59.1 mL
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE12 [hp_X]  in 59.1 mL
    MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS30 [hp_X]  in 59.1 mL
    NUTMEG (UNII: AEE24M3MQ9) (NUTMEG - UNII:AEE24M3MQ9) NUTMEG6 [hp_X]  in 59.1 mL
    PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS12 [hp_X]  in 59.1 mL
    SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE12 [hp_X]  in 59.1 mL
    SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY) (SUS SCROFA NASAL MUCOSA - UNII:ID3Z1X61WY) SUS SCROFA NASAL MUCOSA9 [hp_X]  in 59.1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 41.359658 mL  in 59.1 mL
    ALCOHOL (UNII: 3K9958V90M) 8.862784 mL  in 59.1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 8.862784 mL  in 59.1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64578-0093-159.1 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/21/2014
    Labeler - Energetix Corp (969572502)
    Establishment
    NameAddressID/FEIBusiness Operations
    Terra Botanica LLC963736785manufacture(64578-0093) , label(64578-0093) , pack(64578-0093)