Indications and uses
for relief of occasional sleeplessness when associated with minor aches and pains helps you fall asleep and stay asleep
for relief of occasional sleeplessness when associated with minor aches and pains helps you fall asleep and stay asleep
do not take more than directed drink a full glass of water with each dose adults and children 12 years and over: take 2 tablets at bedtime do not take more than 2 tablets in 24 hours if taken with food, this product may take longer to work Other information read all warnings and directions before use. Keep outer carton. each tablet contains: sodium 20 mg Tamper-evident : do not use if carton is opened or foil sea...
Drug Facts
| Diphenhydramine hydrochloride, USP 25 mg |
| Naproxen sodium, USP 220 mg (naproxen 200 mg) (NSAID)* |
| *nonsteroidal anti-inflammatory drug |
Nighttime sleep-aid/Pain reliever
Allergy alert
Naproxen sodium may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:
If an allergic reaction occurs, stop use and seek medical help right away.
Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:
Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.
ask a health professional before use. It is especially important not to use naproxen sodium during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.
In case of overdose, get medical help or contact a Poison Control Center right away.
Other information
FD&C Blue # 2 Aluminum Lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol 3350, povidone titanium dioxide
1-800-432-8534 between 9 am and 4 pm EST, Monday – Friday.
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 45963-220 | 45963-220-20, 45963-220-40, 45963-220-23, 45963-220-12, 45963-220-24 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | TC2D6JAD40 | ACTIB |
| NAPROXEN SODIUM | 9TN87S3A3C | ACTIB |
| FD&C BLUE NO. 2 | L06K8R7DQK | IACT |
| HYPROMELLOSES | 3NXW29V3WO | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| POLYETHYLENE GLYCOL 3350 | G2M7P15E5P | IACT |
| POVIDONE | FZ989GH94E | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
| CELLULOSE, MICROCRYSTALLINE | OP1R32D61U | IACT |
| ALUMINUM OXIDE | LMI26O6933 | IACT |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 090ca040-1df1-412e-ae5a-8e2f7dbd9cf0 | a7fa26f0-11df-4ddd-ae93-bf640372318b | 2021-10-21 | Warnings | a7fa26f0-11df-4ddd-ae93-bf640372318b |
Adverse event summaries are temporarily unavailable. Other product information remains available.