Severe Anefrin Nasal Spray No Drip MAXIMUM STRENGTH 12 Hour Menthol

Manufacturer
WALGREENS
Effective date
2024-12-11
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:46:54

Label at a glance#

ProductSevere Anefrin
Active ingredientOXYMETAZOLINE HYDROCHLORIDE
Label structure12 sections

Indications and uses

• temporarily relives nasal congestions due to: • common cold • hay fever • upper respiratory allergies • temporarily relieves sinus congestgions 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. • children under 6 years of age: ask a doctor

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Oxymetazoline hydrochloride 0.05%

Warnings Ask a doctor before use if you have

WARNINGS SECTION

• heart disease • high blood pressure • thyroid disease • diabetes • trouble urinating due to an enlarged prostate gland

When using this product • do not use more than directed

WARNINGS SECTION

• do not use for more than 3 days. Use only as directed. Frequent or prolonged use may cause nasla congestion to recur or worsen. • temporary discomfort such as burning, stinging, sneezing or an increase in nasla 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,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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. • children under 6 years of age: ask a doctor

To Use:

INDICATIONS & USAGE SECTION

Shake well before use. Hold white tabs, press grooved area of cap firmly and turn counterclockwise. Before using the firsst time, prime metered pump by depressing pump firmly several times. To spray, hold bottle with thumn 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 nozzle clean after use. Secure cap after use.

DISTRIBUTED BY: WALGREENS CO. 200 WILMOT RD., DEERFIELD, IL 60015

SPL UNCLASSIFIED SECTION

100% SATISFACTION GUARANTEED

walgreens.com ©2020 Walgreen Co.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Benzalkonium Chloride Solution, Camphor, CArboxymethyl Cellulose Sodium, Cellulose Gum, Disodium EDTA, Disodium Phosphate, Eucalyptol, Glycerin, Menthol, Microcrystalline Cellulose, PEG-6, Povidone, Propylene Glycol, Purified Water, Sodium Phosphate Monobasic

Uses

INDICATIONS & USAGE SECTION

• temporarily relives nasal congestions due to:

• common cold • hay fever • upper respiratory allergies

• temporarily relieves sinus congestgions and pressure

• shrinks swollen nasal membranes so you can breath more freely

PURPOSE

OTC - PURPOSE SECTION

Nasal Decongestant

Severe Anefrin Nasal Spray

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NO DRIP

MAXIMUM STRENGTH

12 HOUR

+ MENTHOL

severe anefrinsevere anefrin

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-2021SEVERE ANEFRIN (OXYMETAZOLINE HYDROCHLORIDE) LIQUID [WALGREENS]5Legacy NDC20241213_b637e03a-dc2b-92a3-e053-2995a90a9a6b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-20210363-2021-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
471ae14b-db44-d4d2-e063-6294a90af58eb637e03a-dc2b-92a3-e053-2995a90a9a6b2025-12-29WarningsExact identifier
spl set id: b637e03a-dc2b-92a3-e053-2995a90a9a6b

Reported adverse events (FAERS/openFDA)#

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