All Day Relief 220 mg/1

Naproxen Sodium · CAPSULE, LIQUID FILLED · Publix Supermarkets, Inc.

No Recall History

Plain English

All Day Relief is a capsule, liquid filled containing naproxen sodium at 220 mg/1, taken oral. Manufactured by Publix Supermarkets, Inc..

Key Facts

Brand Name: All Day Relief
Generic Name: Naproxen Sodium
NDC Code (Product): 56062-748
Manufacturer: Publix Supermarkets, Inc.
Strength: 220 mg/1
Dosage Form: CAPSULE, LIQUID FILLED
Route: ORAL
Marketing Status
Application #: ANDA208363
Marketing Start: 06/30/2019

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective2,910 reports

fatigue2,621 reports

off label use2,508 reports

pain2,447 reports

rash2,243 reports

diarrhoea2,201 reports

arthralgia2,196 reports

vomiting2,130 reports

condition aggravated2,100 reports

joint swelling2,059 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses • temporarily relieves minor aches and pains due to: • minor pain of arthritis • muscular aches • backache • menstrual cramps • headache • toothache • the common cold • temporarily reduces fever

Dosage & Administration

Directions • do not take more than directed • the smallest effective dose should be used • drink a full glass of water with each dose Adults and children 12 years and older • take 1 tablet every 8 to 12 hours while symptoms last • for the first dose you may take 2 tablets within the first hour • do not exceed 2 tablets in any 8- to 12-hour period • do not exceed 3 tablets in a 24-hour period Children under 12 years • ask a doctor

Warnings

Warnings Allergy alert: Naproxen sodium may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: • hives • facial swelling • asthma (wheezing) • shock • skin reddening • rash • blisters 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: • are age 60 or older • have had stomach ulcers or bleeding problems • take a blood thinning (anticoagulant) or steroid drug • take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others) • have 3 or more alcoholic drinks every day while using this product • take more or for a longer time than directed 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. Do not use • if you have ever had an allergic reaction to any other pain reliever/fever reducer • right before or after heart surgery Ask a doctor before use if • the stomach bleeding warning appl…

Frequently Asked Questions

What is All Day Relief used for?

All Day Relief contains Naproxen Sodium. It is a capsule, liquid filled taken oral. Consult your doctor for specific uses.

Is All Day Relief a controlled substance?

All Day Relief is not classified as a controlled substance by the DEA.

What is the generic name for All Day Relief?

The generic name for All Day Relief is Naproxen Sodium. There are 12 other brand versions of Naproxen Sodium.

What is the NDC code for All Day Relief 220 mg/1?

The NDC (National Drug Code) for All Day Relief 220 mg/1 is 56062-748, listed by Publix Supermarkets, Inc..

Product NDC

56062-748

Package NDC

56062-748-40

Other Naproxen Brands

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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)