MAX STR.NASAL RELIEF SEVERE CONGESTION- oxymetazoline hydrochloride 0.05% liquid

Max Str.Nasal Relief Severe Congestion by

Drug Labeling and Warnings

Max Str.Nasal Relief Severe Congestion by is a Otc medication manufactured, distributed, or labeled by Ride Aid, Product Quest Mfg, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient                                       Purpose

Oxymetazoline Hydrochloride 0.05%        Nasal decongestant

PURPOSE

INDICATIONS & USAGE

Uses

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

Warnings

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

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.

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

Directions

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

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MAX STR.NASAL RELIEF SEVERE CONGESTION 
oxymetazoline hydrochloride 0.05% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-1232
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Oxymetazoline Hydrochloride (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY)	Oxymetazoline Hydrochloride	0.05 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7)
Benzyl Alcohol (UNII: LKG8494WBH)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
Edetate Disodium (UNII: 7FLD91C86K)
Eucalyptol (UNII: RV6J6604TK)
Menthol (UNII: L7T10EIP3A)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
Povidone (UNII: FZ989GH94E)
Propylene Glycol (UNII: 6DC9Q167V3)
Water (UNII: 059QF0KO0R)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-1232-1	1 in 1 CARTON	05/09/2014
1		15 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	05/09/2014

Labeler - Ride Aid (014578892)

Registrant - Product Quest Mfg, LLC (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg, LLC		927768135	manufacture(11822-1232) , label(11822-1232)