NO DRIP NASAL MIST- oxymetazoline spray liquid 
Walgreens Company

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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Anefrin Nasal Spray Extra Moisturizing  

Drug Facts

Active Ingredient
Oxymetazoline Hydrochloride 0.05%

Purpose

Nasal Decongestant

Uses

Temporarily relieves nasal congestion due to:

Warnings

Ask a Doctor before use if you have

When using this product

stop use and ask a doctor if

symptoms persist.

if pregnant or breast-feeding 

ask a health professional before use.

Keep out of the reach of children

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

Directions

Other information

Inactive Ingredients

Benzalkonium Chloride Solution, Benzyl Alcohol, Edetate Disodium, Flavor, Glycerin, Microcrystalline Cellulose and Carboxymethylcellulose Sodium, Polyethylene Glycol, Povidone, Purified Water, Sodium Phosphate Dibasic, Sodium Phosphate Monobasic

Principal Panel 0.5 FLOZ Bottle

Principal Panel 0.5 FLOZ Bottle

Walgreen    No Drip Nasal Mist 

Extra Moisturizing

Nasal Spray 

Oxymetazoline HCL 0.05%

12 hour Nasal Spray

Net Wt 0.5 FLOZ (15ml)

Principal Panel 0.5 FLOZ Bottle

Principal Panel 0.5 FLOZ Bottle

Principal Panel 0.5 FLOZ Bottle

Principal Panel 0.5 FLOZ Bottle

Principal display panel- Carton label

Walgreens  No Drip Nasal Mist

Extra Moisturizing

Nasal Spray

Oxymetazoline HCL 0.05%

12 hour Nasal Spray

Net Wt 0.5 FLOZ (15ml)

Principal display panel- Carton label

Principal display panel- Carton label

NO DRIP NASAL MIST 
oxymetazoline spray liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-2307
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE50 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
WATER (UNII: 059QF0KO0R)  
POVIDONE (UNII: FZ989GH94E)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-2307-521 in 1 CARTON10/08/2018
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 finalpart34110/08/2018
Labeler - Walgreens Company (008965063)

Revised: 10/2018
Document Id: 7741f87c-5391-4482-a41c-b284112835f3
Set id: 234bd567-4e3c-419f-a000-fdfc28cafc8b
Version: 1
Effective Time: 20181008
 
Walgreens Company