ValuMeds Nasal Decongestant PE Phenylephrine

ValuMeds Nasal Decongestant PE Phenylephrine is an FDA-registered drug product whose active ingredient is PHENYLEPHRINE HYDROCHLORIDE. It is labelled by Cabinet Health P.B.C. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 82725-1011, application M012, label effective 20260710. It is one of 44 FDA drug label records sharing the active ingredient PHENYLEPHRINE HYDROCHLORIDE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing PHENYLEPHRINE HYDROCHLORIDE are most often described in connection with: temporarily relieves, sinus congestion, common cold, hay fever, upper respiratory. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses temporarily relieves sinus congestion and pressure temporarily relieves 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

Warnings Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs fordepression, 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 a MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you hav 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)

FDA lists 44 drug label records with PHENYLEPHRINE HYDROCHLORIDE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is ValuMeds Nasal Decongestant PE Phenylephrine used for?
Uses temporarily relieves sinus congestion and pressure temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies

Who makes ValuMeds Nasal Decongestant PE Phenylephrine?
Cabinet Health P.B.C. is the labeler of record for ValuMeds Nasal Decongestant PE Phenylephrine. 44 FDA label records share the active ingredient PHENYLEPHRINE HYDROCHLORIDE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does ValuMeds Nasal Decongestant PE Phenylephrine come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is ValuMeds Nasal Decongestant PE Phenylephrine prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing PHENYLEPHRINE HYDROCHLORIDE?
Yes. 44 FDA drug label records list PHENYLEPHRINE HYDROCHLORIDE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has ValuMeds Nasal Decongestant PE Phenylephrine been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.