Drugplain

Advil 200 mg/1

IBUPROFEN · TABLET, COATED · JC World Bell Wholesale Co., Inc.

10 Recalls on Record
Plain English

Advil is a tablet, coated containing ibuprofen at 200 mg/1, taken topical. Manufactured by JC World Bell Wholesale Co., Inc..

Key Facts

Brand Name
Advil
Generic Name
IBUPROFEN
NDC Code (Product)
50269-157
Manufacturer
JC World Bell Wholesale Co., Inc.
Strength
200 mg/1
Dosage Form
TABLET, COATED
Route
TOPICAL
Marketing Status
Application #
NDA018989
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing Start
05/18/1984

Recall History

10 Recalls on Record
Class II03/31/2023

Family Dollar Stores, Llc.

CGMP deviation: product outside labeled storage temperature requirements.

OngoingVoluntary: Firm initiated
Class II03/16/2020

Glaxosmithkline Consumer Healthcare Holdings

Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.

TerminatedVoluntary: Firm initiated
Class II03/16/2020

Glaxosmithkline Consumer Healthcare Holdings

Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.

TerminatedVoluntary: Firm initiated
Class II03/16/2020

Glaxosmithkline Consumer Healthcare Holdings

Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.

TerminatedVoluntary: Firm initiated
Class I12/06/2022

Glaxosmithkline Consumer Healthcare Holdings DBA Haleon

Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back

TerminatedVoluntary: Firm initiated
Class II03/31/2023

Family Dollar Stores, Llc.

CGMP deviation: product outside labeled storage temperature requirements.

OngoingVoluntary: Firm initiated
Class I12/06/2022

Glaxosmithkline Consumer Healthcare Holdings DBA Haleon

Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back

TerminatedVoluntary: Firm initiated
Class II08/23/2018

Pfizer Global Supply

Labeling Error: Not elsewhere classified. product has a dosage cup marked in teaspoons and the instructions on the label are described in milliliters.

TerminatedVoluntary: Firm initiated
Class II03/31/2023

Family Dollar Stores, Llc.

CGMP deviation: product outside labeled storage temperature requirements.

OngoingVoluntary: Firm initiated
Class II12/26/2025

GOLD STAR DISTRIBUTION INC

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

OngoingVoluntary: Firm initiated

Side Effects Reported to FDA

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

drug ineffective25,005 reports
pain17,447 reports
fatigue17,153 reports
nausea16,164 reports
headache14,704 reports
arthralgia12,396 reports
dyspnoea11,923 reports
vomiting11,457 reports
diarrhoea11,440 reports
rash10,270 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses ​Uses temporarily relieves minor aches and pains due to: headache toothache backache menstrual cramps muscular aches minor pain of arthritis

Dosage & Administration

Directions ​Directions Do not take more than directed adults and children 12 years and over take 2 caplets every 8 hours while symptoms persist children under 12 years ask a doctor do not take more than 6 caplets in 24 hours, unless directed by a doctor

Warnings

Warnings ​Warnings Acetaminophen liver damage warning Acetaminophen liver damage warning: This product contains acetaminophen. Severe liver damage may occur if you take: with other drugs containing acetaminophen more than 6 caplets in 24 hours, which is the maximum daily amount for this product 3 or more alcoholic drinks every day while using this product Acetaminophen allergy alert Acetaminophen allergy alert: may cause severe skin reactions. Symptoms may include: skin reddening blisters rash If skin reaction occurs, stop use and seek medical help right away. NSAID allergy alert NSAID allergy alert: ibuprofen 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. NSAID stomach bleeding warning NSAID 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 no

Frequently Asked Questions

What is Advil used for?

Advil contains IBUPROFEN. It is a tablet, coated taken topical. Consult your doctor for specific uses.

Is Advil a controlled substance?

Advil is not classified as a controlled substance by the DEA.

What is the generic name for Advil?

The generic name for Advil is IBUPROFEN. There are 11 other brand versions of IBUPROFEN.

What is the NDC code for Advil 200 mg/1?

The NDC (National Drug Code) for Advil 200 mg/1 is 50269-157, listed by JC World Bell Wholesale Co., Inc..