NASAL RELIEF- puraflex nasorelief spray liquid

Nasal Relief by

Drug Labeling and Warnings

Nasal Relief by is a Otc medication manufactured, distributed, or labeled by Shandong Huawei Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

MAGNOLIA BIONDII FLOWER   2%

Purpose

Nasal Decongestant

Uses

For the temporary relief of nasal congestion due to:

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

WARNINGS

Do not use

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

When using this product

• do not share dispenser
• do not exceed recommended dosage

Stop use and ask a doctor if

• condition worsens
• if symptoms persist.

Ask a doctor before use if

• 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:

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

Directions

• 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

Store between 20°-25°C (68°-77°F)

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

Inactive ingredients

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

Questions or comments? (602) 368-7231

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 

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

Made in China

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NASAL RELIEF 
puraflex nasorelief spray liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84246-577
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MAGNOLIA BIONDII FLOWER (UNII: G1YA92798O) (MAGNOLIA BIONDII FLOWER - UNII:G1YA92798O)	MAGNOLIA BIONDII FLOWER	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
XANTHIUM SIBIRICUM FRUIT (UNII: 3H333L84C2)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
ASARUM HETEROTROPOIDES ROOT (UNII: Q94BWI90CD)
BORNEOL (UNII: M89NIB437X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84246-577-30	1 in 1 PACKAGE	04/12/2024
1		30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/12/2024

Labeler - Shandong Huawei Pharmaceutical Co., Ltd. (417377581)

Registrant - Shandong Huawei Pharmaceutical Co., Ltd. (417377581)

Establishment
Name	Address	ID/FEI	Business Operations
Shandong Huawei Pharmaceutical Co., Ltd.		417377581	manufacture(84246-577)