REBOOST LEMON FLU SYMPTOM RELIEF (REBOOST FLU SYMPTOM RELIEF) TABLET, CHEWABLE [MEDINATURA INC]

REBOOST LEMON FLU SYMPTOM RELIEF (REBOOST FLU SYMPTOM RELIEF) TABLET, CHEWABLE [MEDINATURA INC]
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NDC 62795-1036-2
Set ID 3398af9c-c5b0-086b-e054-00144ff8d46c
Category HUMAN OTC DRUG LABEL
Packager MediNatura Inc
Generic Name
Product Class
Product Number
Application Number
  • 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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