NASAL DECONGESTANT EXTRA MOISTURIZING- oxymetazoline hcl spray 
Kareway Product, Inc.

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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Pure-Aid Nasal Spray Extra-Moisturizing

Active ingredient

Oxymetazoline HCl 0.05%

Purpose

Nasal decongestant

Uses

Warnings

Do not use this product for more than 3 days

Ask a doctor before use if you have

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

When using this product

  • do not exceed recommended dosage
  • use only as directed. frequent of prolonged use may cause nasal congestion to recur or worsen
  • temporary discomfort such as burning, stinging, 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

adults and children 6 to under 12 years of age (with adult supervision)2 or 3 spray in each nostril not more often than every 10 to 12 hours
children under 6 years of ageask a doctor






Other information

Inactive ingredients

benzalkonium chloride, concentrated glycerin, edetate disodium, purified water

Carton image

Nasal Spray Extra Moisturizing

carton

NASAL DECONGESTANT EXTRA MOISTURIZING 
oxymetazoline hcl spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67510-0069
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE0.05 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67510-0069-51 in 1 BOX07/03/2013
115 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2NDC:67510-0069-11 in 1 BOX07/03/2013
230 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34108/12/2011
Labeler - Kareway Product, Inc. (121840057)

Revised: 9/2021
Document Id: cc0d5dc8-5936-44f9-e053-2a95a90a2a20
Set id: 3f3a6a24-5c21-44b2-84a7-9c23dd33cc9b
Version: 6
Effective Time: 20210915
 
Kareway Product, Inc.