Influenzinum

Manufacturer
Boiron | Boiron, Inc.
Effective date
2020-11-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:09:06

Label at a glance#

ProductInfluenzinum
Active ingredientINFLUENZA A VIRUS A/SINGAPORE/INFIMH-16-0019/2016 IVR-186 (H3N2) HEMAGGLUTININ ANTIGEN (FORMALDEH..., INFLUENZA B VIRUS B/MARYLAND/15/2016 BX-69A ANTIGEN (FORMALDEHYDE INACTIVATED), INFLUENZA A VIRUS A/MICHIGAN/45/2015 X-275 (H1N1) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED)
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Influenzinum 8X HPUS

A/Michigan/45/2015 (H1N1) pdm09-like virus
A/Singapore/INFIMH-16–0019/2016 (H3N2)-like virus
B/Maryland/15/2016/ BX-69A (B/Colorado/06/2017-like virus (B/Victoria lineage))

OTC - PURPOSE SECTION

Relieves after effects of flu or flu-like symptoms

INDICATIONS & USAGE SECTION

Relieves after effects of flu or flu-like symptoms

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

DOSAGE & ADMINISTRATION SECTION

Unit dose: Dissolve entire contents of the tube under the tongue, repeat as necessary up to 3 times a day

Multi-dose: 5 pellets 3 times a day until symptoms are relieved

SPL UNCLASSIFIED SECTION

Multi-dose:

Do not use if pellet dispenser seal is broken

Approx 80 pellets

These "Uses" have not been evaluated by the FDA

Unit Dose:

Do not use if cap seal is broken or missing

Store at 68-77 degrees F

These "Uses" have not been evaluated by the FDA

INACTIVE INGREDIENT SECTION

lactose, sucrose

OTC - QUESTIONS SECTION

Made in France

Distributed by Boiron Inc.

1-800-BOIRON-1

Newtown Square, PA 19073

info@Boiron.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-26520220-2652-41, 0220-2652-31

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b9bd4fd3-32f7-e1f7-e053-2a95a90a0eec76126c7e-5c1d-3bb5-e053-2a91aa0adc452021-01-25Exact identifier
spl set id: 76126c7e-5c1d-3bb5-e053-2a91aa0adc45

Reported adverse events (FAERS/openFDA)#

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