OXYMETAZOLINE HYDROCHLORIDE description, usages, side effects, indications, overdosage, supplying and lots more!

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OXYMETAZOLINE HYDROCHLORIDE

Rebel Distributors Corp

Nasal Decongestant Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Oxymetazoline HCl 0.05%

Purpose

Nasal decongestant

Keep Out of Reach of Children

If swallowed, get medical help or contact a Poison Control Center right away.

OXYMETAZOLINE HYDROCHLORIDE Uses

temporary relief of nasal congestion

° due to the common cold

° due to hay fever or other upper respiratory allergies

° associated with sinusitis

reduces swelling of nasal passages

temporarily restores freer breathing through the nose

Warnings

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.

Ask a doctor before use if you have:

° heart disease ° high blood pressure

° thyroid disease ° diabetes

° difficulty in urination due to enlargement of the prostate gland

When using this product, frequent or prolonged use may cause nasal congestion to recur or worsen.

Stop use and ask a doctor if symptoms persist.

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

Directions

° Adults and children 6 to under 12 years of age (with supervision): 2 to 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 spray: squeeze the bottle quickly and firmly. Do not tilt head backward while spraying. Wipe nozzle clean after use.

Inactive ingredients

benzalkonium chloride, dibasic sodium phosphate (anhydrous), edetate disodium (dihydrate), monobasic sodium phosphate (monohydrate), polyethylene glycol 1450, povidone, propylene glycol, purified water.

Questions? Cal 1-866-923-4914

Package/Label Principal Display Panel

OXYMETAZOLINE HYDROCHLORIDE

OXYMETAZOLINE HYDROCHLORIDE

OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:21695-875(NDC:51672-2030)
Route of Administration NASAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OXYMETAZOLINE HYDROCHLORIDE OXYMETAZOLINE 0.5 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
SODIUM PHOSPHATE, DIBASIC ANHYDROUS
EDETATE DISODIUM
Sodium Phosphate, Monobasic, Monohydrate
POLYETHYLENE GLYCOL 1450
povidone
propylene glycol
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:21695-875-15 15 in 1 BOTTLE, SPRAY
2 NDC:21695-875-30 30 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2008-12-11


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Be sure to consult your doctor before taking any medication!
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