Nostrilla

Nostrilla is an FDA-registered drug product whose active ingredient is OXYMETAZOLINE HYDROCHLORIDE. It is labelled by Insight Pharmaceuticals LLC taken by nasal and marketed as a human otc drug product. Identifiers on file: NDC 63736-730, application M012, label effective 20260904. It is one of 44 FDA drug label records sharing the active ingredient OXYMETAZOLINE 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 OXYMETAZOLINE HYDROCHLORIDE are most often described in connection with: temporarily relieves, nasal congestion, due cold, hay fever, upper respiratory, allergies helps, passages shrinks, swollen membranes. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses temporarily relieves nasal congestion due to: ▪ a cold ▪ hay fever ▪ upper respiratory allergies ▪ helps clear nasal passages; shrinks swollen membranes ▪ temporarily restores freer breathing through the nose

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 Squeeze and unscrew to remove the protective cap. Align rail grooves and prime pump by depressing it firmly several times (see illustration on side). Hold bottle with thumb at base and nozzle between first and second fingers. With head upright, insert nozzle into nostril. Depress pump two or three times, all the way down, and sniff deeply.

Warnings Ask a doctor before use if you have heart disease thyroid disease high blood pressure diabetes trouble urinating due to an enlarged prostate gland When using this product do not exceed recommended dosage temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge may occur do not use for more than 3 days. Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen. use of this container by more than one person may spread infection Stop use and ask a doctor if symptoms persist If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

FDA lists 44 drug label records with OXYMETAZOLINE 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.

4 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 Nostrilla used for?
Uses temporarily relieves nasal congestion due to: ▪ a cold ▪ hay fever ▪ upper respiratory allergies ▪ helps clear nasal passages; shrinks swollen membranes ▪ temporarily restores freer breathing through the nose

Who makes Nostrilla?
Insight Pharmaceuticals LLC is the labeler of record for Nostrilla. 44 FDA label records share the active ingredient OXYMETAZOLINE 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 Nostrilla 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 Nostrilla 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 OXYMETAZOLINE HYDROCHLORIDE?
Yes. 44 FDA drug label records list OXYMETAZOLINE 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 Nostrilla been recalled?
4 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.