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OTC products · Product label record

Vicks Sinex SEVERE CONGESTION MOISTURIZING ULTRA FINE MIST drug information

OXYMETAZOLINE HYDROCHLORIDE
Procter & Gamble Manufacturing GmbH · NASAL

Product NDC: 64336-004

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameOXYMETAZOLINE HYDROCHLORIDE
Labeler / manufacturerProcter & Gamble Manufacturing GmbH
RouteNASAL
Drug classDrug class not supplied in source label
Product NDC64336-004
Label effective date2026-08-24

Official product label reference

Vicks Sinex SEVERE CONGESTION MOISTURIZING ULTRA FINE MIST — Procter & Gamble Manufacturing GmbH

This page contains 15 source sections for OXYMETAZOLINE HYDROCHLORIDE, nasal route. Label set 464534ee-15f8-3af8-e063-6394a90a3f18, version 4.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses temporarily relieves nasal congestion due to a cold, hay fever, or other upper respiratory allergies sinus congestion and pressure

Purpose

Purpose Nasal decongestant
Dosage and administration — label text
Directions Remove protective cap. Before using for the first time, prime the pump by firmly depressing its rim several times. Hold container with thumb at base and nozzle between first and second fingers. Without tilting your head, insert nozzle into nostril. Fully depress rim with a firm, even stroke and inhale deeply. adults & children 6 yrs. & older (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 24 hours. children 2 to under 6 yrs. ask a doctor children under 2 yrs. do not use Table text from source: | adults & children 6 yrs. & older (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 24 hours. | children 2 to under 6 yrs. | ask a doctor | children under 2 yrs. | do not use
Warnings
Warnings Ask a doctor before use if you have heart disease thyroid disease diabetes high blood pressure trouble urinating due to enlarged prostate gland
Unclassified section
Drug Facts Only selected information is listed on the bottle label. Keep this carton for future reference. TAMPER EVIDENT: CARTON SEALED FOR YOUR PROTECTION. MADE IN GERMANY DIST. BY PROCTER & GAMBLE, CINCINNATI OH 45202
Active ingredient
Active ingredient Oxymetazoline HCl 0.05%
Ask a doctor before use
Ask a doctor before use if you have heart disease thyroid disease diabetes high blood pressure trouble urinating due to enlarged prostate gland
While using this medicine
When using this product do not exceed recommended dosage do not use this product 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 increased nasal discharge may occur use of this container by more than one person may spread infection
When to stop use and seek help
Stop use and ask a doctor if symptoms persist.
Pregnancy or breast feeding
If pregnant or breast-feeding, ask a health professional before use.
Child safety
Keep out of reach of children.
Overdose information
If swallowed, get medical help or contact a Poison Control Center right away
Storage and handling
Other information store at no greater than 25°C
Inactive ingredient
Inactive ingredients acesulfame potassium, aloe, benzalkonium chloride, benzyl alcohol, citric acid anhydrous, edetate disodium, fragrance, polysorbate 80, purified water, sodium citrate, sorbitol.
Questions
Questions? 1-800-873-8276

Official sources and product identifiers

Substances listed: OXYMETAZOLINE HYDROCHLORIDE

RxNorm identifiers: 1000990

Package NDC codes

64336-004-01, 64336-004-02, 64336-004-03

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.