NO DRIP NASAL
NO DRIP NASAL is an FDA drug label for the active ingredient PHENYLEPHRINE HYDROCHLORIDE manufactured by CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED administered by NASAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260622.
- Generic name
- PHENYLEPHRINE HYDROCHLORIDE
- Manufacturer
- CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
- Product type
- HUMAN OTC DRUG
- Route
- NASAL
- Dosage form
- N/A
- NDC
- 51316-648
- Application
- M012
- Label effective
- 20260622
About this product
NO DRIP NASAL is an FDA-registered drug product whose active ingredient is PHENYLEPHRINE HYDROCHLORIDE. It is labelled by CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED taken by nasal and marketed as a human otc drug product. Identifiers on file: NDC 51316-648, application M012, label effective 20260622. 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.
What it is used for
Across FDA labelling, products containing PHENYLEPHRINE HYDROCHLORIDE are most often described in connection with: temporarily relieves, nasal congestion, due common, cold hay, fever upper, respiratory allergies, pressure shrinks. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses • temporarily relieves nasal congestion due to: • common cold • hay fever • upper respiratory allergies • temporarily relieves sinus congestion and pressure • shrinks swollen nasal membranes so you can breathe more freely
Dosage & Administration
Directions • adults and children 12 years of age and over: 2 or 3 sprays in each nostril not more often than every 4 hours. • children under 12 years of age: ask a doctor To Use: Shake well before use. Hold white tabs, SQUEEZE grooved area of cap FIRMLY and turn counter clockwise. Before using the first time, prime 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.
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 • 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 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 right away (1-800-222-1222).
More products with the same ingredient
PHENYLEPHRINE HYDROCHLORIDECVS Health Four Actions Nasal Decongestant
View labelEphrine Nose Drops
View labelEquate Nasal
View labelExtra Strength Nasal
View labelGoodMeds Nasal Decongestant
View labelNASAL
View labelNasal
View labelHow products containing PHENYLEPHRINE HYDROCHLORIDE compare
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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | BF ASCHER AND CO INC | 4 |
| — | — | Medical Purchasing Solutions, LLC | 4 |
| — | — | Cabinet Health P.B.C. | 2 |
| — | — | HHH Pharmaceuticals | 2 |
| — | — | Lifestar Pharma LLC | 2 |
Recall and safety notices
5 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.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0623-2022 | No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, Distributed by SUPERVALU INC., Eden Prairie, MN 55344 USA. NDC 41163-703-10 | Perrigo Company PLC | Class II | Terminated | 20220302 |
| D-0624-2022 | Maximum Strength No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202. NDC 30142-388-10 | Perrigo Company PLC | Class II | Terminated | 20220302 |
| D-0615-2022 | No Drip Nasal Mist, Oxymetazoline HCl 0.05% Nasal decongestant, 1 FL Oz (30 mL) per bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC 59779-388-10 | Perrigo Company PLC | Class II | Terminated | 20220302 |
| D-0613-2022 | Maximum Strength No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: AMAZON.COM SERVICES LLC, 410 TERRY AVENUE N. SEATTLE, WA 9810. NDC 72288-388-10 | Perrigo Company PLC | Class II | Terminated | 20220302 |
| D-0606-2022 | Severe Congestion No Drip Nasal Spray Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY DOLGENCORP, LLC, 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072. NDC 55910-511-10 | Perrigo Company PLC | Class II | Terminated | 20220302 |
Frequently asked questions
What is NO DRIP NASAL used for?
Uses • temporarily relieves nasal congestion due to: • common cold • hay fever • upper respiratory allergies • temporarily relieves sinus congestion and pressure • shrinks swollen nasal membranes so you can breathe more freely
Who makes NO DRIP NASAL?
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED is the labeler of record for NO DRIP NASAL. 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 NO DRIP NASAL 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 NO DRIP NASAL 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 NO DRIP NASAL been recalled?
5 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.