Label: AFRIN NO DRIP NIGHT CHAMOMILE- oxymetazoline hydrochloride spray, metered

  • NDC Code(s): 11523-1160-1, 11523-1160-2
  • Packager: Bayer HealthCare LLC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 15, 2023

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Active ingredientsPurpose
    Oxymetazoline hydrochloride 0.05%Nasal decongestant

  • Purpose

  • Uses

    Uses

    • temporarily relieves nasal congestion due to:
      • common cold
    • hay fever
    • upper respiratory allergies
    • shrinks swollen nasal membranes so you can breathe more

    freely

    • temporarily relieves sinus congestion and pressure
  • Warnings

    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

    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

    Stop use and ask a doctor if

    Stop use and ask a doctor if symptoms persist

    If pregnant or breast-feeding

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

    Keep out of reach of children

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

    Directions

    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. Secure cap after use.

  • Other information

    Other information

    • store between 20º to 25ºC (68º to 77ºF)
    • retain carton for future reference on full labeling
  • Inactive ingredients

    Inactive ingredients 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

  • Questions or comments

    Questions or comments? 1-800-317-2165

  • Package label

    11523-1160NEW

    Oxymetazoline HCl

    Nasal Solution-Nasal Decongestant

    Afrin®

    NoDrip

    Won't drip from nose or down throat

    Night

    with soothing chamomile scent

    PUMP MIST

    Instant

    Congstion

    Relief for a

    More Restful

    Night

    Up to 12

    HOUR

    RELIEF

    Colds · Allergies

    #1 Doctor Recommended

    Nasal Decongestant Spray

    1/2 FL OZ (15 mL)

  • INGREDIENTS AND APPEARANCE
    AFRIN NO DRIP NIGHT  CHAMOMILE
    oxymetazoline hydrochloride spray, metered
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-1160
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE0.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
    POVIDONE (UNII: FZ989GH94E)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11523-1160-10.5 mL in 1 BOTTLE, PUMP; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)07/01/202007/01/2020
    2NDC:11523-1160-21 in 1 CARTON07/01/2020
    215 mL in 1 BOTTLE, PUMP; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/01/2020
    Labeler - Bayer HealthCare LLC. (112117283)