All Day Pain Relief 220 mg/1

Naproxen Sodium · TABLET · H E B

No Recall History

Plain English

All Day Pain Relief is a tablet containing naproxen sodium at 220 mg/1, taken oral. Manufactured by H E B.

Key Facts

Brand Name: All Day Pain Relief
Generic Name: Naproxen Sodium
NDC Code (Product): 37808-068
Manufacturer: H E B
Strength: 220 mg/1
Dosage Form: TABLET
Route: ORAL
Marketing Status
Application #: ANDA079096
Marketing Start: 09/30/2015

Recall History

No Recall History

Side Effects Reported to FDA

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

drug ineffective2,873 reports

fatigue2,619 reports

off label use2,508 reports

pain2,448 reports

rash2,238 reports

arthralgia2,196 reports

diarrhoea2,196 reports

vomiting2,126 reports

condition aggravated2,101 reports

joint swelling2,057 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 caplet every 8 to 12 hours while symptoms last • for the first dose you may take 2 caplets within the first hour • do not exceed 2 caplets in any 8- to 12-hour period • do not exceed 3 caplets 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 appli…

Frequently Asked Questions

What is All Day Pain Relief used for?

All Day Pain Relief contains Naproxen Sodium. It is a tablet taken oral. Consult your doctor for specific uses.

Is All Day Pain Relief a controlled substance?

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

What is the generic name for All Day Pain Relief?

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

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

The NDC (National Drug Code) for All Day Pain Relief 220 mg/1 is 37808-068, listed by H E B.

Product NDC

37808-068

Package NDC

37808-068-24

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)