Max Str.Nasal Relief Severe Congestion

Manufacturer
Ride Aid | Product Quest Mfg, LLC
Effective date
2018-06-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:00

Label at a glance#

ProductMax Str.Nasal Relief Severe Congestion
Active ingredientOxymetazoline Hydrochloride
Label structure6 sections

Dosage and administration

Before using the first time, remove the protective cap from the tip and prime 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. • adults and children 6 to under12 years of age (with adult supervi...

Label contents#

Full prescribing information#

Active ingredient                                       Purpose

OTC - ACTIVE INGREDIENT SECTION

Oxymetazoline Hydrochloride 0.05%        Nasal decongestant

INDICATIONS & USAGE SECTION

Uses

• for the temporary relief of nasal congestion due to
the common cold, hay fever or other upper respiratory
allergies

Warnings

WARNINGS SECTION

Ask a doctor before use if you have
• 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 this product if you have heart disease • high
blood pressure • thyroid disease • diabetes • or difficulty
in urination due to enlargement of the prostate gland
When using this product • Do not exceed recommended
dosage. • This product may cause temporary
discomfort such as burning, stinging, sneezing, or an
increase in nasal discharge. • The use of this
container by more than one person may spread
infection. • Do not use for more than 3 days. Use only as
directed. • Frequent or prolonged use may cause nasal
congestion to recur or worsen.
Stop use and ask doctor if symptoms persist,
consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a PoisonControl Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Before using the first time, remove the protective cap from the tip and prime 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. • adults and children 6 to under12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 10 to 1 2 hours. Do not exceed 2 doses within any 24-hour period • children under 6 years of age: consult a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION


Benzalkonium Chloride, Benzyl Alcohol, Camphor, Edetate Disodium, Eucalyptol, Menthol, Microcrystalline Cellulose, Polyethylene Glycol, Povidone, Propylene Glycol, Purified Water, Sodium Carboxymethyl Cellulose, Sodium Phosphate Dibasic, Sodium Phosphate Monobasic.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1000990oxymetazoline HCl 0.05 % Nasal SprayPSN1
1000990oxymetazoline hydrochloride 0.5 MG/ML Nasal SpraySCD1
1000990oxymetazoline hydrochloride 0.05 % Nasal SpraySY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
OXYMETAZOLINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
e67be450-f8e4-4bc1-88bd-1259d379f55fProduct name120210127
c53f3286-4062-4cf5-8355-399519c639a6Product name120170424
a993dfc5-f219-4460-bde6-30dd724d9ef0Product name120160818
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-1232-12020-01-31C16284748780-19d75b9d0-d585-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-1232-1Max Str.Nasal Relief Severe Congestion1 in 1 CARTONLIQUID11
11822-1232-1Max Str.Nasal Relief Severe Congestion15 mL in 1 BOTTLELIQUID151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-1232MAX STR.NASAL RELIEF SEVERE CONGESTION (OXYMETAZOLINE HYDROCHLORIDE 0.05%) LIQUID [RIDE AID]1Legacy NDC, 2 package rows20180619_edee5cb8-7ca4-494e-a97d-ac82f47638d7.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-123211822-1232-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
63bb5640-d8d3-43d4-9c1e-009a8d91a260edee5cb8-7ca4-494e-a97d-ac82f47638d72018-06-18WarningsExact identifier
spl id: 63bb5640-d8d3-43d4-9c1e-009a8d91a260
spl set id: edee5cb8-7ca4-494e-a97d-ac82f47638d7

Reported adverse events (FAERS/openFDA)#

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