FDA.reportPublic FDA data

VALUHEALTH Nasal Solution NO DRIP

Manufacturer
ACCENT PHARMA
Effective date
2026-08-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-01 13:02:51

Label at a glance#

ProductOxymetazoline hydrochloride nasal solution
Active ingredientOXYMETAZOLINE HYDROCHLORIDE
Label structure9 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 membranes so you can breathe 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. To use: Shake well before use. Hold white tabs, Press grooved area of cap firmly and turn counter clockwise. then remove the clip. Before using the first time, remove the protective ...

Storage and handling

store between 20-25°C (68° - 77°F)

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

  • Temporarily relieves nasal congestion due to:
    • common cold
    • hay fever
    • upper respiratory allergies
  • temporarily relieves sinus congestion and pressure
  • Shrinks swollen membranes so you can breathe more freely

WARNINGS SECTION

Warning

Ask Doctor before use if you have

OTC - ASK DOCTOR SECTION

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

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.

OTC - STOP USE SECTION

Stop use and ask Doctor if Symptoms persist

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the 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.
  • 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. then remove the clip.

Before using the first time, remove the protective cap from the tip and 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 and clip after use.

Other information

STORAGE AND HANDLING SECTION

  • store between 20-25°C (68° - 77°F)

INACTIVE INGREDIENT SECTION

benzalkonium chloride solution, benzyl alcohol, carboxymethyl cellulose sodium, edetate disodium, flavour, microcrystalline cellulose, polyethylene glycol, povidone, purified water, sodium phosphate dibasic, sodium phosphate monobasic.

OTC - QUESTIONS SECTION

​Questions or comments? 1-888-333-9792

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton

Carton LabelCarton Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810151110363GTIN-13: 0810151110363
EAN-13: 0810151110363
GTIN-12: 810151110363
UPC-A: 810151110363
GTIN storage (14 digits): 00810151110363		Prodose_No Drip Nasal Spray Carton.jpg

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87265-004987265-0049-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
OXYMETAZOLINE HYDROCHLORIDEK89MJ0S5VYACTIB
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS22ADO53M6FIACT
BENZYL ALCOHOLLKG8494WBHIACT
EDETATE DISODIUM7FLD91C86KIACT
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUSKH7I04HPUUIACT
WATER059QF0KO0RIACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311IACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
POVIDONEFZ989GH94EIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-08-13daily-update2026-08-20 01:01:14

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
5a19e8bb-c82b-b2ec-e063-6294a90a573a58e88fa2-d5c0-bcde-e063-6294a90af6012026-08-28WarningsExact identifier
spl id: 5a19e8bb-c82b-b2ec-e063-6294a90a573a
spl set id: 58e88fa2-d5c0-bcde-e063-6294a90af601

Reported adverse events (FAERS/openFDA)#

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