AVON HEXASHIELD CONGESTION RELIEF ORIGINAL- oxymetazoline hydrochloride spray 
Tai Guk Pharm. Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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AVON HeXashield Nasal Relief Spray Congestion Relief Original

Active Ingredient

Oxymetazoline HCl 0.05%

Purpose

Nasal decongestant

Uses

- common cold - hay fever

- upper respiratory allergies

Warnings

For external use only.

Ask a doctor before use if you have

  • heart disease
  • high blood pressure
  • diabetes
  • thyroid disease
  • trouble urinating due to an enlarged prostate gland

When using this product

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

Stop use and ask a doctor if :

  • symptoms persist.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions

Other information

Inactive Ingredients

benzalkonium chloride, edetate disodium, polyethylene glycol 400, povidone, propylene glycol, sodium phosphate dibasic, sodium phosphate monobasi dihydrate, water

Questions or comments?

Call toll free 1-800-FOR-AVON

www.avon.com

Principal Display Panel

HeXasheild

ORIGINAL

NASAL RELIEF SPRAY

CONGESTION RELIEF

Oxymetazoline HCl-

Nasal Decongestant

Compare to the active ingredient in Afrin ® Original

Rapid & Powerful Congestion

Relief 12 Hour Relief

AVON

NET WT 0.5 FL oz (15 mL)

AVON NASAL RELIEF SPRAY

AVON HEXASHIELD CONGESTION RELIEF  ORIGINAL
oxymetazoline hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43136-105
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43136-105-011 in 1 CARTON07/31/2019
115 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34107/31/2019
Labeler - Tai Guk Pharm. Co., Ltd. (689060246)
Establishment
NameAddressID/FEIBusiness Operations
Tai Guk Pharma. Co., Ltd.689060246manufacture(43136-105)

Revised: 7/2019
Document Id: 8f2c1590-b311-56d6-e053-2995a90a4ab2
Set id: 8f2c152c-c564-0cba-e053-2a95a90ab3c7
Version: 1
Effective Time: 20190731
 
Tai Guk Pharm. Co., Ltd.