Afrin No Drip Night

Manufacturer
Delpharm Montreal Inc.
Effective date
2020-10-27
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:09:43

Label at a glance#

ProductAfrin No Drip Night Chamomile
Active ingredientOXYMETAZOLINE HYDROCHLORIDE
Label structure8 sections

Indications and uses

Uses temporarily relieves nasal congestion due to: common cold hay fever upper respiratory allergies Reduces swelling of nasal passages so you can breathe more freely temporarily relieves sinus congestion and pressure Uses section was updated to reflect the artwork approved by the product owner Bayer (artwork approved on 24aug2020).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Active ingredientsPurpose
Oxymetazoline hydrochloride 0.05%Nasal decongestant

Uses

INDICATIONS & USAGE SECTION

Uses

  • temporarily relieves nasal congestion due to:
    • common cold
  • hay fever
  • upper respiratory allergies
  • Reduces swelling of nasal passages so you can breathe more

freely

  • temporarily relieves sinus congestion and pressure

RECENT MAJOR CHANGES SECTION

Uses section was updated to reflect the artwork approved by the product owner Bayer (artwork approved on 24aug2020).

Warnings

WARNINGS SECTION

Warnings

Ask a doctor before use if you have

•heart disease • high blood pressure

•thyroid disease • diabetes

•trouble urinating due to an enlarged prostate gland

When using this product

OTC - WHEN USING SECTION

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 burning, 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

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

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

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.

  • children 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 the first time, prime metered pump by depressing pump 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 nozzle clean after use. Secure cap after use.

Other information

OTHER SAFETY INFORMATION

Other information

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients benzalkonium chloride solution, benzyl alcohol, dibasic sodium phosphate, edetate disodium, flavor, glycerin, microcrystalline cellulose and carboxymethylcellulose sodium, monobasic sodium phosphate, polyethylene glycol, povidone, purified water

Questions or comments

OTC - QUESTIONS SECTION

Questions or comments? 1-800-317-2165

Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

69213-1160-269213-1160-2

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69213-116069213-1160-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
b2a8ea58-f874-4b6c-e053-2995a90a9721a52501f0-1fba-6471-e053-2995a90aed722020-10-27WarningsExact identifier
spl id: b2a8ea58-f874-4b6c-e053-2995a90a9721
spl set id: a52501f0-1fba-6471-e053-2995a90aed72

Reported adverse events (FAERS/openFDA)#

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