Rinosan MINT Nasal Decongestant Spray

Manufacturer
Bee Right LLC
Effective date
2018-07-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:53:42

Label at a glance#

ProductRinosan MINT Nasal Decongestant
Active ingredientEPHEDRINE HYDROCHLORIDE
Label structure7 sections

Indications and uses

temporarily relieves nasal congestion due to the common cold, hay fever (allergic rhinitis) temporarily relieves stuffy nose; temporarily restores freer breathing reduces swelling of nasal passages; shrinks swollen membranes helps decongest sinus openings and passages; temporarily relieves sinus congestion and pressure promotes nasal and/or sinus drainage

Dosage and administration

 Adults and children 12 year of age and over  2 or 3 sprays in each nostril not more than once every 4 hours  Children 6 to under 12 years of age (with adult supervision)  1 or 2 sprays in each nostril not more than once every 4 hours  Children under 6 years of age  Consult a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ephedrine Hydrochloride 0.5%

Purpose

OTC - PURPOSE SECTION

Nasal Decongestant

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves nasal congestion due to the common cold, hay fever (allergic rhinitis)
  • temporarily relieves stuffy nose; temporarily restores freer breathing
  • reduces swelling of nasal passages; shrinks swollen membranes
  • helps decongest sinus openings and passages; temporarily relieves sinus congestion and pressure
  • promotes nasal and/or sinus drainage

Warnings

WARNINGS SECTION

Consult a doctor before use if you have:

• heart disease • high blood pressure • thyroid disease • diabetes • difficulty in urination due to enlargement of the prostate gland 

When using this product

OTC - WHEN USING SECTION

  • use of this container by more than one person may spread infection
  • this product may cause temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge
  • do not use this product for more than 3 days; use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen

Do not

OTC - DO NOT USE SECTION

  • exceed recommended  dosage

Stop use and consult a doctor if:

OTC - STOP USE SECTION

symptoms persist

If pregnant or breastfeeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

consult a health care professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

 Adults and children 12 year of age and over 2 or 3 sprays in each nostril not more than once every 4 hours
 Children 6 to under 12 years of age (with adult supervision) 1 or 2 sprays in each nostril not more than once every 4 hours
 Children under 6 years of age Consult a doctor

Other information

SPL UNCLASSIFIED SECTION

  • store in a dry and dark place at room temperature
  • use within 30 days of opening

Inactive ingredients

INACTIVE INGREDIENT SECTION

Benzalkonium chloride, calcium chloride, disodium phosphate, eucalyptus globulus oil, menthol, potassium chloride, sodium chloride, water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Package3Outer Package3Inner Package3Inner Package3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71952-030-002021-01-29C16284748780-1ba0f9c33-37ce-a910-e053-dadaa90a0b85Rinosan MINT Nasal Decongestant Spray

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71952-030RINOSAN MINT NASAL DECONGESTANT (EPHEDRINE HYDROCHLORIDE) SPRAY [BEE RIGHT LLC]3Legacy NDC20180703_1239e824-aa60-4b7f-9910-81f96ebe6c70.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
71952-03071952-030-00

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
701603fa-befe-111c-e053-2991aa0ae2b41239e824-aa60-4b7f-9910-81f96ebe6c702018-07-03WarningsExact identifier
spl id: 701603fa-befe-111c-e053-2991aa0ae2b4
spl set id: 1239e824-aa60-4b7f-9910-81f96ebe6c70

Reported adverse events (FAERS/openFDA)#

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