Label: REBOOST- apis mellifera, atropa belladonna, zinc gluconate, baptisia tinctoria root, ulmus rubra bark, sulfur, zinc acetate anhydrous,vincetoxicum hirundinaria root and cairina moschata heart/liver spray
- NDC Code(s): 62795-4004-9
- Packager: MediNatura
- 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 August 8, 2022
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ACTIVE INGREDIENTS
Each 20ml contains
Active Ingredients Purpose
*Apis mellifica 6X 1.25%
*Asclepias Vincetoxicum 6X 10X 30X 1.25%
*Belladonna 5X 1.25%
*Organic Calendula officinalis 4X 1.25%
*Organic Echinacea purpurea 4X 1.25%
*Hydrastis canadensis 5X 1.25%
*Phytolacca decandra 4X 1.25%
*Plantago major 3X 1.25%
*Salvia officinalis 3X 1.25%
*Zincum Gluconlcum 1X 2.5%
*Wild Harvested Baptisia Tinctoria 1X 1.25%
*Ulmus Fulva 1X 1.25%
*Sulphur 4X 10X 1.25%
*Zincum Aceticum 4X 2.5%
*Anas Barbariae 20X 200C 1.25%
*Natural Ingredients
- INACTIVE INGREDIENTS
- USES
- DIRECTIONS
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WARNINGS
Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a health professional promptly. Do not use more than 2 days. This product contains ethanol and should not be inhaled. In rare cases allergic reactions may occur. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. The use of this a by more than one person may spread infection. 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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- INDICATIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
REBOOST
apis mellifera, atropa belladonna, zinc gluconate, baptisia tinctoria root, ulmus rubra bark, sulfur, zinc acetate anhydrous,vincetoxicum hirundinaria root and cairina moschata heart/liver sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62795-4004 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 6 [hp_X] in 20 mL ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 5 [hp_X] in 20 mL CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP 4 [hp_X] in 20 mL ECHINACEA PURPUREA (UNII: QI7G114Y98) (ECHINACEA PURPUREA - UNII:QI7G114Y98) ECHINACEA PURPUREA 4 [hp_X] in 20 mL GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 5 [hp_X] in 20 mL PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG) PHYTOLACCA AMERICANA ROOT 4 [hp_X] in 20 mL PLANTAGO MAJOR (UNII: W2469WNO6U) (PLANTAGO MAJOR - UNII:W2469WNO6U) PLANTAGO MAJOR 3 [hp_X] in 20 mL SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J) SAGE 3 [hp_X] in 20 mL ZINC GLUCONATE (UNII: U6WSN5SQ1Z) (ZINC CATION - UNII:13S1S8SF37) ZINC GLUCONATE 1 [hp_X] in 20 mL BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU) BAPTISIA TINCTORIA ROOT 1 [hp_X] in 20 mL ULMUS RUBRA BARK (UNII: 91QY4PXU8Q) (ULMUS RUBRA BARK - UNII:91QY4PXU8Q) ULMUS RUBRA BARK 1 [hp_X] in 20 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 4 [hp_X] in 20 mL ZINC ACETATE ANHYDROUS (UNII: H2ZEY72PME) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 4 [hp_X] in 20 mL VINCETOXICUM HIRUNDINARIA ROOT (UNII: 9R858U917W) (CYNANCHUM VINCETOXICUM ROOT - UNII:9R858U917W) VINCETOXICUM HIRUNDINARIA ROOT 6 [hp_X] in 20 mL CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE - UNII:RN2HC612GY) CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 20 [hp_X] in 20 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) FRUCTOSE (UNII: 6YSS42VSEV) WATER (UNII: 059QF0KO0R) CHERRY (UNII: BUC5I9595W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62795-4004-9 1 in 1 CARTON 02/05/2020 1 20 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/05/2020 Labeler - MediNatura (079324099) Establishment Name Address ID/FEI Business Operations MediNatura 102783016 manufacture(62795-4004)