NeilMed Sinufrin Quick Relief Decongestant

Manufacturer
Neilmed pharmaceuticals Inc.
Effective date
2026-08-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-08-08 02:01:05

Label at a glance#

ProductSinufrin Quick Relief Decongestant
Active ingredientOXYMETAZOLINE
Label structure12 sections

Indications and uses

Temporarily relieves nasal congestion due to: Common cold Hay fever Upper respiratory allergies Temporarily relieves sinus congestion and pressure Shrinks swollen nasal membranes so you can breathe more freely

Dosage and administration

Adults and children 6 to under 12 years of age (with adult supervision): 3 or 4 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: Push firmly down on cap and turn counter clockwise. To spray, squeeze bottle quickly and firmly. Do not tilt head backward while spraying. Wipe nozzle clean after use. Secure ...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Oxymetazoline hydrochloride 0.04% Active IngredientsActive Ingredients

Purpose

OTC - PURPOSE SECTION

Nasal Decongestant PurposePurpose

Uses:

INDICATIONS & USAGE SECTION

  • Temporarily relieves nasal congestion due to:
  • Common cold
  • Hay fever
  • Upper respiratory allergies
  • Temporarily relieves sinus congestion and pressure
  • Shrinks swollen nasal membranes so you can breathe more freely Indications and UsesIndications and Uses

Warnings

WARNINGS SECTION

Ask a doctor before use if you have

  • Heart disease
  • High blood pressure
  • Diabetes
  • Thyroid disease
  • Trouble urinating due to an enlarged prostate gland WarningsWarnings

When using this product

OTC - WHEN USING SECTION

  • 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. When using this productWhen using this product

Warnings

OTC - STOP USE SECTION

​Stop use and ask a doctor if symptoms persist Stop UseStop Use

Warnings

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

Warnings

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. Keep out of reach of childrenKeep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 6 to under 12 years of age (with adult supervision): 3 or 4 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: Push firmly down on cap and turn counter clockwise. To spray, squeeze bottle quickly and firmly. Do not tilt head backward while spraying. Wipe nozzle clean after use. Secure cap after use. Dosage and AdministrationDosage and Administration

OTHER SAFETY INFORMATION

Other Information

  • Store between 68° F (20° C) and 86° F (30° C)
  • Retain carton for future reference on full labeling Other InformationOther Information

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium chloride, sodium bicarbonate, propylene glycol, edetate disodium, benzalkonium chloride, purified water. Inactive IngredientsInactive Ingredients

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Packaging label principal display panelsPackaging label principal display panels

Package label

DailyMed Product Concepts#

Product concept, Relation, Version table
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
13709-325-012024-01-31C16284748780-11030e365-6335-111a-e063-dadaa90a10e2NeilMed Sinufrin Quick Relief Decongestant
13709-325-012024-01-31C16284748780-11030e365-6335-111a-e063-dadaa90a10e2NeilMed Sinufrin Quick Relief Decongestant

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
13709-32513709-325-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-01-09full-release2026-06-01 00:08:07

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
Sinufrin Quick Relief DecongestantSINUFRINNeilmed pharmaceuticals Inc.0c36a34e-462d-713c-e063-6294a90a17762026-08-05WarningsExact identifier
ndc (package): 13709-325-01
ndc (product): 13709-325
ndc11 (package): 13709032501
spl id: 584b8a64-5de5-85ad-e063-6294a90a21a5
spl set id: 0c36a34e-462d-713c-e063-6294a90a1776

Reported adverse events (FAERS/openFDA)#

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