FDA.reportPublic FDA data

Nasal Relief

Manufacturer
Shandong Huawei Pharmaceutical Co., Ltd.
Effective date
2024-05-15
Label type
HUMAN OTC DRUG LABEL
Version
32896
Source
full-release
Hydrated at
2026-06-01 00:12:37

Label at a glance#

ProductNasal Relief
Active ingredientMAGNOLIA BIONDII FLOWER
Label structure14 sections

Indications and uses

For the temporary relief of nasal congestion due to: common cold sinusitis upper respiratory allergies respiratory tract infections weather changes

Dosage and administration

With the head held upright, remove the protective cap. Insert the spray nozzle into the nostril.  Depress the pump completely 1-3 times.  Sniff gently. Repeat up to 3 times daily.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

MAGNOLIA BIONDII FLOWER   2%

Purpose

OTC - PURPOSE SECTION

Nasal Decongestant

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of nasal congestion due to:

  • common cold
  • sinusitis
  • upper respiratory allergies
  • respiratory tract infections
  • weather changes

WARNINGS

WARNINGS SECTION

Do not use

  • on eyes
  • if excessive irritation develops
  • if allergic to any of the ingredients

When using this product

OTC - WHEN USING SECTION

  • do not share dispenser
  • do not exceed recommended dosage

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

  • condition worsens
  • if symptoms persist.

Ask a doctor before use if

OTC - ASK DOCTOR/PHARMACIST SECTION

  • you have serious chronic diseases
  • you are pregnant or breast-feeding
  • you are menstruating
  • you are using for your children under 3 years of age.

Keep out of reach of children. Overdose Warning:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

  • With the head held upright, remove the protective cap.
  • Insert the spray nozzle into the nostril. 
  • Depress the pump completely 1-3 times. 
  • Sniff gently. Repeat up to 3 times daily.

Other information

OTHER SAFETY INFORMATION

• Store between 20°-25°C (68°-77°F)

• The container is filled to proper level for best spray action.

Inactive ingredients

INACTIVE INGREDIENT SECTION

MAGNOLIA BIONDII FLOWER, XANTHIUM SIBIRICUM FRUIT, ANGELICA DAHURICA ROOT, ASARUM HETEROTROPOIDES ROOT, BORNEOL, PURIFIED WATER

Questions or comments? (602) 368-7231

OTC - QUESTIONS SECTION

M-F, 9:30 am to 5:30 pm Pacific Time
You may also report serious side effects to this phone number.

Manufactured for Heshoutang Products LLC 

SPL UNCLASSIFIED SECTION

9035 N 43rd Ave, Phoenix, AZ 85051, USA
www.heshoutang.com

Made in China

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84246-577-30Nasal Relief1 in 1 PACKAGELIQUID132896
84246-577-30Nasal Relief30 mL in 1 BOTTLE, SPRAYLIQUID3032896

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84246-577NASAL RELIEF (PURAFLEX NASORELIEF SPRAY) LIQUID [SHANDONG HUAWEI PHARMACEUTICAL CO., LTD.]328962 package rows20240517_4d79dad3-7258-4f09-8782-56ec6a1629ba.zip

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
84246-57784246-577-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
MAGNOLIA BIONDII FLOWERG1YA92798OACTIB
XANTHIUM SIBIRICUM FRUIT3H333L84C2IACT
ANGELICA DAHURICA ROOT1V63N2S972IACT
ASARUM HETEROTROPOIDES ROOTQ94BWI90CDIACT
BORNEOLM89NIB437XIACT
WATER059QF0KO0RIACT

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
263c903e-8b55-4fe7-a837-39e61b726cc74d79dad3-7258-4f09-8782-56ec6a1629ba2024-05-15WarningsExact identifier
spl id: 263c903e-8b55-4fe7-a837-39e61b726cc7
spl set id: 4d79dad3-7258-4f09-8782-56ec6a1629ba

Reported adverse events (FAERS/openFDA)#

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