Anefrin Nasal Spray NO DRIP ORIGINAL 12 HOUR MAXIMUM STRENGTH

Drug Details [pdf]

NO DRIP ANEFRIN NASAL- oxymetazoline hydrochloride liquid
WALGREENS

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Anefrin Nasal Spray

NO DRIP
ORIGINAL
12 HOUR
MAXIMUM STRENGTH

Drug Facts

ACTIVE INGREDIENT

Oxymetazoline hydrochloride 0.05%

Purpose

Nasal decongestant

Uses

temporaily relieves nasal congestion due to:
common cold
hay fever
upper respiratory allergires
temporarily relieves sinus congestion and pressure
shrinks swollen nasal membranes so you can breath more freely

Warnings

Ask a doctor before use if you have

heart disease
high blood pressure
thyroid disease
diabetes
trouble urinating due to an enlarged prostrate 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 buring, 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

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.
childer under 6 years of age: ask a doctor.

To Use: Shake well before use. Hold white tabs, press grooved area of cap firmly and turn counter clockwise. Before using for the first time, prime metered pump by depressing firmly several times. To spray, hold bottle with thumb at base and nozzle between first and second fingers. Without tilting head, insert nozzle into nostril. Fully depress rim with a firm, even stroke and sniff deeply. Wipe nozel clean after use.

Secure cap after use.

Other information

store between 20º to 25ºC (68º to 77ºF)
retain carton for future reference on full labeling

Inactive ingredients

benzalkonium chloride solution, carboxymethylcellulose sodium solution, edetate disodium, glycerin, microcrystalline cellulose, polyethylene glycol 300, povidone, propylene glycol, purified water, sodium phosphate dibasic, sodium phosphate monobasic

Questions or comments?

1-800-925-4733

15 mL Bottle Carton

Anefrin Nasal Spray

NO DRIP

ORGINIAL

12 HOUR

MAXIMUM STRENGTH

Won't drip from nose or down throat
Helps Relieve congestion

0.5 FL OZ (15 mL)

anefrin nasal spray no drip

NO DRIP ANEFRIN NASAL
oxymetazoline hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-7007
Route of Administration	NASAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY)	OXYMETAZOLINE HYDROCHLORIDE	0.05 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POVIDONE K30 (UNII: U725QWY32X)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 0363-7007-15	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/26/2021	08/31/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M012	02/26/2021	08/31/2023

Labeler - WALGREENS (008965063)

Revised: 10/2023

Document Id: 0905369d-99b4-26e7-e063-6294a90aa571

Set id: b6234e99-115f-6018-e053-2a95a90a6989

Version: 3

Effective Time: 20231031