Anefrin Nasal Spray NO DRIP ORIGINAL 12 HOUR MAXIMUM STRENGTH

Manufacturer
WALGREENS | MEDICAL PRODUCTS LABORATORIES, INC.
Effective date
2021-02-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:49:57

Label at a glance#

ProductNo Drip Anefrin Nasal
Active ingredientOXYMETAZOLINE HYDROCHLORIDE
Label structure10 sections

Indications and 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

Dosage and administration

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 s...

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Oxymetazoline hydrochloride 0.05%

Purpose

OTC - PURPOSE SECTION

Nasal decongestant

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

1-800-925-4733

15 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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 dripanefrin nasal spray no drip

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-70070363-7007-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0905369d-99b4-26e7-e063-6294a90aa571b6234e99-115f-6018-e053-2a95a90a69892023-10-31WarningsExact identifier
spl set id: b6234e99-115f-6018-e053-2a95a90a6989

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.