NASAL RELIEF- puraflex nasorelief spray liquid 
Shandong Huawei Pharmaceutical Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Shandong Huawei Pharmaceutical Co., Ltd.

Active Ingredients

MAGNOLIA BIONDII FLOWER   2%

Purpose

Nasal Decongestant

Uses

For the temporary relief of nasal congestion due to:

WARNINGS

Do not use

When using this product

Stop use and ask a doctor if

Ask a doctor before use if

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

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

image description

NASAL RELIEF 
puraflex nasorelief spray liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84246-577
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNOLIA BIONDII FLOWER (UNII: G1YA92798O) (MAGNOLIA BIONDII FLOWER - UNII:G1YA92798O) MAGNOLIA BIONDII FLOWER2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
XANTHIUM SIBIRICUM FRUIT (UNII: 3H333L84C2)  
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)  
ASARUM HETEROTROPOIDES ROOT (UNII: Q94BWI90CD)  
BORNEOL (UNII: M89NIB437X)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84246-577-301 in 1 PACKAGE04/12/2024
130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/12/2024
Labeler - Shandong Huawei Pharmaceutical Co., Ltd. (417377581)
Registrant - Shandong Huawei Pharmaceutical Co., Ltd. (417377581)
Establishment
NameAddressID/FEIBusiness Operations
Shandong Huawei Pharmaceutical Co., Ltd.417377581manufacture(84246-577)

Revised: 5/2024
Document Id: 263c903e-8b55-4fe7-a837-39e61b726cc7
Set id: 4d79dad3-7258-4f09-8782-56ec6a1629ba
Version: 32896
Effective Time: 20240515
 
Shandong Huawei Pharmaceutical Co., Ltd.