Label: REBOOST LEMON FLU SYMPTOM RELIEF- reboost flu symptom relief tablet, chewable
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Contains inactivated NDC Code(s)
NDC Code(s): 62795-1036-2 - Packager: MediNatura Inc
- 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
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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)