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Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)
Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)
Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)
Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)
Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)
Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)
Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)
Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)
Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)
Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)

Sudafed PE Maximum Strength Non-Drowsy Sinus Congestion Tablets, 10 mg, (18 count)

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Product Summary

Description

Sudafed PE Congestion Maximum Strength Sinus + Nasal Congestion Relief provides non-drowsy relief from both sinus congestion and pressure caused by colds or allergies. With phenylephrine HCl, a nasal decongestant, the product temporarily relieves sinus congestion and pressure and nasal congestion due to the common cold, hay fever, or other upper-respiratory allergies.

Directions

Adults and children 12 years and over: take 1 tablet every 4 hours. Do not take more than 6 tablets in 24 hours.

Children under 12 years: ask a doctor.

Ingredients

Active: Phenylephrine HCl 10 mg

Inactive: Carnauba Wax, D&C Yellow No. 10 Aluminum Lake, FD&C Red No. 40 Aluminum Lake, FD&C Yellow No.

6 Aluminum Lake, Magnesium Stearate, Microcrystalline Cellulose, Modified Starch, Polyethylene Glycol, Polyvinyl Alcohol,

Powdered Cellulose, Pregelatinized Starch, Sodium Starch Glycolate, Talc, Titanium Dioxide

Warnings and Restrictions

  • Do not use if carton or blister unit is opened or broken.
  • Keep this box for important information.
  • Does not contains pseudoephedrine.
  • Important: Read all product information before using.

DO NOT USE if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

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 EXCEED RECOMMENDED DOSE.

STOP USE AND ASK A DOCTOR IF:

  • nervousness, dizziness, or sleeplessness occur
  • symptoms do not improve within 7 days or occur with a fever

IF PREGNANT OR BREAST-FEEDING: ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.

(1-800-222-1222)

Storage

Store between 20-25C (68-77F).

Other Information

Company Name: Johnson & Johnson Consumer Inc.

Company Address: McNeil Consumer Healthcare Division, Fort Washington, PA, 19034, USA.

Customer Services

Return To:

Johnson & Johnson Consumer Inc.,

McNeil Consumer Healthcare Division,

Fort Washington, PA, 19034, USA.

Questions or comments?

Call 1-888-217-2117 (toll-free) or 215-273-8755 (collect)

Attachments

Patient Information Leaflet
App Store
Google Play
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Version 2.32.6
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