- KEET OUT OF REACH OF CHILDREN
- USES
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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.
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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
- INACTIVE INGREDIENTS
- Purpose
- ReBoost Cold & Flu Symptom Tablets
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INGREDIENTS AND APPEARANCE
REBOOST LEMON FLU SYMPTOM RELIEF
reboost flu symptom relief tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62795-1036 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS 4 [hp_X] GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 6 [hp_X] EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E) EUPATORIUM PERFOLIATUM FLOWERING TOP 3 [hp_X] LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 10 [hp_X] PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 8 [hp_X] ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID 8 [hp_X] BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 3 [hp_X] Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) 1 g LACTOSE (UNII: J2B2A4N98G) 1 g STEVIA LEAF (UNII: 6TC6NN0876) 1 g Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor LEMON Imprint Code Sun Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62795-1036-2 1 in 1 CARTON 05/24/2016 1 100 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/24/2016 Labeler - MediNatura Inc (079324099) Establishment Name Address ID/FEI Business Operations MediNatura 102783016 manufacture(62795-1036)