EXTRA MOISTURIZING NO DRIP NASAL WALGREENS- oxymetazoline hydrochloride - 0.05% liquid 
Walgreens

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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Drug Facts

Active ingredient                                      Purpose

Oxymetazoline Hydrochloride - 0.05%     Nazal Decongestant

Uses

For the temporary relief of nasal congestion due to the common cold, hay fever or other upper respiratory allergies.

Warning

Ask doctor before us if person has heart disease, high blood pressure, thyroid disease, diabetes, or if adult has difficulty in urination due to enlargement of the prostate gland unless directed by a doctor.

When using this product

Do not exceed recommended dosage

Do not use this product for more than 3 days. Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen. If symptoms persist, consult a doctor.This product may cause temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge. The use of this container by more than one person may spread infection.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

Direction

Adults and children 6 to under 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period. Children under 6 years of age: consult a doctor.

Inactive ingredients

Benzalkonium Chloride
Benzyl Alcohol
Cellulose Gum
Disodium EDTA
Disodium Phosphate
Flavor
Glycerin
Microcrystalline Cellulose
PEG-12
Povidone
Sodium Phosphate
Water

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EXTRA MOISTURIZING NO DRIP NASAL  WALGREENS
oxymetazoline hydrochloride - 0.05% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-7004
Route of AdministrationTOPICAL
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)  
Benzyl Alcohol (UNII: LKG8494WBH)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
Glycerin (UNII: PDC6A3C0OX)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)  
Povidone (UNII: FZ989GH94E)  
Sodium Phosphate (UNII: SE337SVY37)  
water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-7004-011 in 1 CARTON07/01/2016
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34107/01/2016
Labeler - Walgreens (008965063)
Registrant - Product Quest Mfg. (927768135)
Establishment
NameAddressID/FEIBusiness Operations
Product Quest Mfg.927768135manufacture(0363-7004) , label(0363-7004)

Revised: 2/2018
Document Id: 77df9152-a348-40a4-b3c1-cfc81f998b0f
Set id: 0fc2571f-dc1a-4e22-b4fe-d8094bcde3d9
Version: 3
Effective Time: 20180214
 
Walgreens