Label: AFRIN NO DRIP PUMP MIST BUNDLE PACK- oxymetazoline hydrochloride kit
- NDC Code(s): 11523-0147-1
- Packager: Bayer HealthCare LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 23, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- trouble urinating due to an enlarged prostate gland
When using this product
- 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
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Directions
- 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. Before using the first time, 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.
- Other information
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Inactive ingredients
No Drip Original
benzalkonium chloride solution, benzyl alcohol, edetate disodium, flavor, microcrystalline cellulose and carboxymethylcellulose sodium, polyethylene glycol, povidone, purified water, sodium phosphate dibasic, sodium phosphate monobasic
No Drip Night
benzalkonium chloride solution, benzyl alcohol, dibasic sodium phosphate, edetate disodium, flavor, glycerin, microcrystalline cellulose and carboxymethylcellulose sodium, monobasic sodium phosphate, polyethylene glycol, povidone, purified water
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PRINCIPAL DISPLAY PANEL - Bundle Pack Carton
BUNDLE PACK 2 X 15 mL Bottles
Oxymetazoline HCl Nasal Solution-Nasal Decongestant
Afrin ®
No DripOriginal
NASAL PUMP MIST
- Relieves Nasal Congestion & Sinus Congestion/Pressure
Unblocks in
SECONDS*
Lasts 12 HRS
1/2 FL OZ (15 mL)
Oxymetazoline HCl Nasal Solution-Nasal Decongestant
Afrin ®
No DripNight
NASAL PUMP MIST
- Nasal Congestion Relief for a More Restful Night
- Chamomile Scent
Unblocks in
SECONDS*
Lasts 12 HRS
1/2 FL OZ (15 mL)
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INGREDIENTS AND APPEARANCE
AFRIN NO DRIP PUMP MIST BUNDLE PACK
oxymetazoline hydrochloride kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11523-0147 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11523-0147-1 1 in 1 CARTON; Type 0: Not a Combination Product 04/19/2024 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE, SPRAY 15 mL Part 2 1 BOTTLE, PUMP 15 mL Part 1 of 2 AFRIN NO DRIP ORIGINAL PUMP MIST
oxymetazoline hydrochloride spray, meteredProduct Information Item Code (Source) NDC:11523-3142 Route of Administration NASAL 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 POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) WATER (UNII: 059QF0KO0R) SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW) EDETATE DISODIUM (UNII: 7FLD91C86K) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) BENZYL ALCOHOL (UNII: LKG8494WBH) POVIDONE (UNII: FZ989GH94E) SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) Product Characteristics Color Score Shape Size Flavor LEMON Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 15 mL in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 08/31/1999 Part 2 of 2 AFRIN NO DRIP NIGHT CHAMOMILE
oxymetazoline hydrochloride spray, meteredProduct Information Item Code (Source) NDC:11523-1160 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE 0.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) WATER (UNII: 059QF0KO0R) SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW) EDETATE DISODIUM (UNII: 7FLD91C86K) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) BENZYL ALCOHOL (UNII: LKG8494WBH) POVIDONE (UNII: FZ989GH94E) SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 15 mL in 1 BOTTLE, PUMP; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 08/31/1999 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/19/2024 Labeler - Bayer HealthCare LLC. (112117283)