Flu-Tone

Manufacturer
Energetix Corp | Apotheca Company
Effective date
2018-05-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:58:20

Label at a glance#

ProductFlu-Tone
Active ingredientCAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, AZADIRACHTA INDICA BARK, BAPTISIA TINCTORIA ROOT, BRYONIA ALBA ROOT, CROTALUS HORRIDUS HORRIDUS VENOM, ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLIATUM FLOWERING TOP, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS ROOT, GINKGO, INFLUENZA A VIRUS A/CALIFORNIA/7/2009 X-181 (H1N1) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED), INFLUENZA A VIRUS A/HONG KONG/4801/2014 X-263B (H3N2) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTI..., INFLUENZA B VIRUS B/BRISBANE/60/2008 HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED), SUS SCROFA NASAL MUCOSA, PHYTOLACCA AMERICANA ROOT, PINUS SYLVESTRIS LEAFY TWIG, RANCID BEEF, SELENIUM, STILLINGIA SYLVATICA ROOT
Label structure9 sections

Indications and uses

Temporary relief of flu symptoms (early, mid-course, or recovery) such as aches, fever, chills, nausea, cough, fatigue, diarrhea.

Dosage and administration

Take 30 drops orally twice daily or as directed by a healthcare professional. Consult a physician for use in children under 12 years of age or if symptoms worsen or persist.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Anas barbariae, Hepatis et cordis extractum 15C, 30C; Azadirachta indica 12X; Baptisia tinctoria 4X; Bryonia (Alba)12X; Crotalus horridus 15X; Echinacea (Angustifolia) 4X; Eupatorium perfoliatum 30X, 30C; Ferrum phosphoricum 12X; Gelsemium sempervirens 6X; Ginkgo biloba 4X; Influenzinum 30X, 30C; Mucosa nasalis suis 9X, 12X, 6C; Phytolacca decandra 4X; Pinus sylvestris 9X; Pyrogenium 30X, 30C; Selenium metallicum 12X; Stillingia sylvatica 4X.

PURPOSE:

OTC - PURPOSE SECTION

Temporary relief of flu symptoms (early, mid-course, or recovery) such as aches, fever, chills, nausea, cough, fatigue, diarrhea.

WARNINGS:

WARNINGS SECTION

In case of overdose, get medical help or call a Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

Other Information

Store at room temperature out of direct sunlight.

Do not use if neck wrap is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Take 30 drops orally twice daily or as directed by a healthcare professional.

Consult a physician for use in children under 12 years of age or if symptoms worsen or persist.

USES:

INDICATIONS & USAGE SECTION

Temporary relief of flu symptoms (early, mid-course, or recovery) such as aches, fever, chills, nausea, cough, fatigue, diarrhea.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Purified Water, Glycerin, 15% Ethyl Alcohol

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by

Energetix Corp

Dahlonega, GA 30533

Questions? Comments?
800.990.7085

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

energetix

Flu-Tone

Homeopathic Remedy

Flu symptoms (early, mid-course, or recovery)

such as aches, fever, chills, nausea, cough,

fatigue, diarrhea.


2 fl oz (59.1 mL)

Flu-ToneFlu-Tone

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64578-013464578-0134-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
013f384a-b444-4de7-8ebe-f4a5bc4b728522b5f0b6-58c3-4902-9401-e22b04ad4e6a2018-05-10WarningsExact identifier
spl id: 013f384a-b444-4de7-8ebe-f4a5bc4b7285
spl set id: 22b5f0b6-58c3-4902-9401-e22b04ad4e6a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.