Sinufrin Plus No Drip Decongestant

Sinufrin Plus No Drip Decongestant is an FDA-registered drug product whose active ingredient is NASAL CONGESTION RELIEF. It is labelled by NeilMed Pharmaceuticals Inc taken by nasal and marketed as a human otc drug product. Identifiers on file: NDC 13709-356, application M012, label effective 20260413. It is one of 2 FDA drug label records sharing the active ingredient NASAL CONGESTION RELIEF. 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 NASAL CONGESTION RELIEF are most often described in connection with: common cold, hay fever, upper respiratory, allergies temporarily, relieves sinus, pressure shrinks, swollen nasal, freely packaging. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Common cold Hay fever Upper respiratory allergies Temporarily relieves sinus congestion and pressure Shrinks swollen nasal membranes so you can breathe more freely Packaging label principal display panels

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: Push firmly down on cap and turn counter clockwise. To spray, squeeze bottle quickly and firmly. Do not tilt head backward while spraying. Wipe nozzle clean after use. Secure cap after use Directions

Warnings 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 When using this product

FDA lists 2 drug label records with NASAL CONGESTION RELIEF 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.

1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is Sinufrin Plus No Drip Decongestant used for?
Uses Common cold Hay fever Upper respiratory allergies Temporarily relieves sinus congestion and pressure Shrinks swollen nasal membranes so you can breathe more freely Packaging label principal display panels

Who makes Sinufrin Plus No Drip Decongestant?
NeilMed Pharmaceuticals Inc is the labeler of record for Sinufrin Plus No Drip Decongestant. 2 FDA label records share the active ingredient NASAL CONGESTION RELIEF, 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 Sinufrin Plus No Drip Decongestant come in?
administered by nasal. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Sinufrin Plus No Drip Decongestant 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 NASAL CONGESTION RELIEF?
Yes. 2 FDA drug label records list NASAL CONGESTION RELIEF 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 Sinufrin Plus No Drip Decongestant been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.