ORIGINAL NO DRIP NASAL- oxymetazoline hydrochloride - 0.05% liquid

Original No Drip Nasal by

Drug Labeling and Warnings

Original No Drip Nasal by is a Otc medication manufactured, distributed, or labeled by Rite Aid, Product Quest Mfg.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient                                  Purpose

Oxymetazoline Hydrochloride - 0.05% Nazal Decongestant

PURPOSE

Uses

Uses
For the temporary relief of nasal congestion due to the
common cold hay fever other upper respiratory
allergies.

Warnings

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 Poison Control Center right away

Direction

Shake well before use. 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 each use.
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: consult a doctor

OTHER SAFETY INFORMATION

Other information
store at room temperature

Inactive ingredients

Benzalkonium Chloride
Benzyl Alcohol
Cellulose Gum
Disodium EDTA
Disodium Phosphate
Flavor
Microcrystalline Cellulose
PEG-12
Povidone
Sodium Phosphate
Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ORIGINAL NO DRIP NASAL 
oxymetazoline hydrochloride - 0.05% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-1231
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)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
Povidone (UNII: FZ989GH94E)
Sodium Phosphate (UNII: SE337SVY37)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-1231-1	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 - Rite Aid (014578892)

Registrant - Product Quest Mfg. (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg.		927768135	manufacture(11822-1231) , label(11822-1231)