RhinAllergy Tablets

Manufacturer
Boiron | Boiron, Inc.
Effective date
2020-02-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:12:25

Label at a glance#

ProductRhinAllergy
Active ingredientAMBROSIA ARTEMISIIFOLIA, SCHOENOCAULON OFFICINALE SEED, EUPHRASIA STRICTA, ONION, SOLIDAGO VIRGAUREA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE
Label structure12 sections

Storage and handling

store at 68-77F (20-25C)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Allium cepa 5C HPUS

Ambrosia artemisiaefolia 5C HPUS

Euphrasia officinalis 5C HPUS

Histaminum hydrochloricum 9C HPUS

Sabadilla 5C HPUS

Solidago virgaurea 5C HPUS

OTC - PURPOSE SECTION

Allium cepa 5C HPUS....relieves runny nose associated with allergies

Ambrosia artemisiaefolia 5C HPUS ...relieves spasmodic cough associated with hay fever

Euphrasia officinalis 5C HPUS ...relieves burning, irritated eyes

Histaminum hydrochloricum 9C HPUS ...relieves symptoms of allergic conditions

Sabadilla 5C HPUS ...relieves sneezing and itchy throat associated with allergies

Solidago virgaurea 5C HPUS ...relieves abundant nasal discharge

INDICATIONS & USAGE SECTION

temporarily relieves one or more of these symptoms of hay fever or other upper respiratory allergies, itchy and watery eyes, sneezing, runny nose, itchy throat and nose

INACTIVE INGREDIENT SECTION

magnesium stearate, lactose, croscarmellose sodium

HOW SUPPLIED SECTION

60 tablets

STORAGE AND HANDLING SECTION

store at 68-77F (20-25C)

OTC - QUESTIONS SECTION

BoironUsa.com

Info@boironusa.com

1-800-BOIRON-1

1-800-264-7661

Distributed by Boiron:

6 Campus Blvd

Newtown Square, PA 19073-3267

OTC - ASK DOCTOR SECTION

ask a doctor before use in children under 2 years of age

OTC - STOP USE SECTION

stop use and ask a doctor if symptoms persist continuously for more than 7 days or worsen

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: at the onset of symptoms, dissolve 2 tablets under the tongue every 15 minutes for 1 hour, then, dissolve 2 tablets under the tongue 3 times a day until symptoms are relieved.

Children 2 to 6 years of age: Dissolve 2 tablets in 1 tablespoon of water for easier intake. Follow directions above.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

boxbox

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-9315-042023-01-30C16284748780-19d75b9d0-aaf5-f424-e053-dadaa90a57ceRhinAllergy Tablets
0220-9315-042020-02-26C16284748780-19d75b9d0-aaf5-f424-e053-dadaa90a57ceRhinAllergy Tablets
0220-9315-042020-01-31C16284748780-19d75b9d0-aaf5-f424-e053-dadaa90a57ceRhinAllergy Tablets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9315-04RhinAllergy60 in 1 BLISTER PACKTABLET602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9315RHINALLERGY (SOLIDAGO VIRGAUREA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, AMBROSIA ARTEMISIIFOLIA, ONION, EUPHRASIA STRICTA, SCHOENOCAULON OFFICINALE SEED) TABLET [BOIRON]2Legacy NDC, 1 package rows20200226_6dd95c00-88cd-bb7c-e053-2991aa0a24b3.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-93150220-9315-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
6dd95c00-88ce-bb7c-e053-2991aa0a24b36dd95c00-88cd-bb7c-e053-2991aa0a24b32018-06-04Exact identifier
spl set id: 6dd95c00-88cd-bb7c-e053-2991aa0a24b3

Reported adverse events (FAERS/openFDA)#

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