Label: REBOOST LEMON FLU SYMPTOM RELIEF- reboost flu symptom relief tablet, chewable

  • 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 17, 2018

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  • KEET OUT OF REACH OF CHILDREN

    KEET OUT OF REACH OF CHILDREN

  • USES

    For the temporary relief of minor cold and flu symptoms: • Congestion •Runny Nose •Body Aches

  • WARNINGS

    In isolated cases allergic skin reactions may occur. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if known sensitivity to Reboost™ or any of its ingredients exists.

  • DIRECTIONS

    At first sign of symptoms:

    Adults and children 12 years and older: Chew 2-3 tablets every 4 hours. Do not exceed 18 tablets in 24 hours.

    Children 4 to 11 years: Chew 1-2 tablets every 4 hours. Do not exceed 18 tablets in 24 hours.

    For children under 4 years, consult your health professional.

    Allow tablets to dissolve completely in the mouth.

  • ACTIVE INGREDIENTS

    *Aconitum napellus 4X, *Bryonia alba 3X*Bryonia alba 3X, *Eupatorium perfoliatum 3X,*Hydrastis canadensis 6X, *Lachesis mutus 10X, and Phosphorus 5X

    *Natural Ingredients

  • INACTIVE INGREDIENTS

    Citric acid, Lactose, Magnesium stearate, Organic Lemon flavor with other natural flavors (4.5%), Organic Stevia (0.1%)

  • Purpose

    Relieves

    • Congestion

    • Runny Nose

    • Body Aches

  • ReBoost Cold & Flu Symptom Tablets

    ReBoost Cold and Flu Symptom Relief Lemon.jpg

  • INGREDIENTS AND APPEARANCE
    REBOOST LEMON FLU SYMPTOM RELIEF 
    reboost flu symptom relief tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62795-1036
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS4 [hp_X]
    GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL6 [hp_X]
    EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E) EUPATORIUM PERFOLIATUM FLOWERING TOP3 [hp_X]
    LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM10 [hp_X]
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS8 [hp_X]
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID8 [hp_X]
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT3 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30) 1 g
    LACTOSE (UNII: J2B2A4N98G) 1 g
    STEVIA LEAF (UNII: 6TC6NN0876) 1 g
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize9mm
    FlavorLEMONImprint Code Sun
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62795-1036-21 in 1 CARTON05/24/2016
    1100 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/24/2016
    Labeler - MediNatura Inc (079324099)
    Establishment
    NameAddressID/FEIBusiness Operations
    MediNatura102783016manufacture(62795-1036)
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