Flurox Flu Spray

Manufacturer
CureImmune Corp.
Effective date
2019-08-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:11:27

Label at a glance#

ProductFlurox Flu
Active ingredientASTRAGALUS NUTTALLII LEAF, GOLDENSEAL, ZINC CARBOBENZOXY-.BETA.-ALANYLTAURINATE, ECHINACEA ANGUSTIFOLIA, ZINC PHOSPHATE, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE
Label structure7 sections

Dosage and administration

Directions for adults and children 15 years of age and older: Take 2 to 4 sprays in mouth weekly for prevention of colds and flu, and take daily during symptoms, or as directed by a health professional. Take at least 5 minutes before or after eating or drinking. See package insert for details.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Anas Barbariae 200CK 61.7%;

Tauroxicum 6X 5.8%

2.5% for each of the following:

Astragalus 6X, 12X, 30X

Echinacea ang 6X, 12X, 30X

Hydrastis 6X, 12X, 30X

Tauroxicum 12X, 30X

Zinc phos, 12X, 30X

Use

INDICATIONS & USAGE SECTION

Immune system support and treatment of fatigue and flu symptoms

OTC - PURPOSE SECTION

Immune system support and treatment of fatigue and flu symptoms

Directions

DOSAGE & ADMINISTRATION SECTION

Directions for adults and children 15 years of age and older: Take 2 to 4 sprays in mouth weekly for prevention of colds and flu, and take daily during symptoms, or as directed by a health professional. Take at least 5 minutes before or after eating or drinking. See package insert for details.

Warnings

WARNINGS SECTION

Warnings

Keep out of reach of children. Do not use if you are pregnant or breast feeding, an organ recipient, using immunosuppressive drugs, or if the tamper-evident seal is broken or missing. See package insert for details.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

20% alcohol (ethanol), purified water

Disclaimer

OTHER SAFETY INFORMATION

Claims based on traditional
homeopathic practice, not accepted
medical evidence. Not FDA evaluated.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Flurox

Flu Spray

Immune system support

and treatment of fatigue

and flu symptoms

With Taurox

An Adaptive MicroMed

and the active ingredient

used in Oscillo®

HOMEOPATHIC

20% alcohol

1 Fl oz (29.5ml)

Flurox front panelFlurox front panel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73311-005-032022-01-28C16284748780-1d6a99b39-ec22-a426-e053-dadaa90af4c2Flurox Flu Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73311-005-03Flurox Flu1 in 1 BAGLIQUID11
73311-005-03Flurox Flu1 in 1 BOTTLE, SPRAYLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73311-005FLUROX FLU (ANAS BARBARIAE, ASTRAGALUS, ECHINACEA ANG, HYDRASTIS, TAUROXICUM, ZINC PHOS) LIQUID [CUREIMMUNE CORP.]1Legacy NDC, 2 package rows20190827_910b0237-94e7-db5a-e053-2a95a90ad703.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73311-00573311-005-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML · Source PDF

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
910b1db9-9cb8-6b19-e053-2a95a90a1964910b0237-94e7-db5a-e053-2a95a90ad7032019-08-26WarningsExact identifier
spl id: 910b1db9-9cb8-6b19-e053-2a95a90a1964
spl set id: 910b0237-94e7-db5a-e053-2a95a90ad703

Reported adverse events (FAERS/openFDA)#

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