Childrens Ibuprofen Oral Suspension, Dye Free (IBUPROFEN)

Best Choice · suspension · NDC 63941-128

Listed in the FDA National Drug Code directory

Childrens Ibuprofen Oral Suspension, Dye Free is an over-the-counter medicine made available by Best Choice, on the U.S. market since January 2025. It is marketed under an FDA approval (ANDA ANDA210602), so the FDA has reviewed its safety, effectiveness and manufacturing. A listing proves the product exists; it does not prove that a particular pack is genuine, so compare yours with the official description below.

What the genuine product looks like

From the official FDA label (version of Jan 20, 2025). Compare the colour, shape, imprint and packaging with what you have. Any difference is a reason to ask a pharmacist before taking it.

Product data on the label: Childrens Ibuprofen Oral Suspension, Dye Free IBUPROFEN IBUPROFEN IBUPROFEN ACESULFAME POTASSIUM ANHYDROUS CITRIC ACID CARBOXYMETHYLCELLULOSE SODIUM GLYCERIN MICROCRYSTALLINE CELLULOSE POLYSORBATE 80 PROPYLENE GLYCOL WATER SODIUM BENZOATE SUCROSE XANTHAN GUM Original Berry

Text on the package panel: -------------- Package Labeling: Best Choice ® Children's Ibuprofen Oral Suspension, Dye Free Best Choice ​® ​ Children's Ibuprofen Oral Suspension (NSAID) 100 mg/5 ml Pain Reliever/Fever Reducer LASTS UP TO 8 HOURS COMPARE TO THE ACTIVE INGREDIENT IN CHILDREN'S MOTRIN ® ** For ages 2 to 11 years Original Berry Flavor 4 FL OZ (11 8 mL) Important Read all product information before using. Keep this box for important information. This product is intended for use in children. **This product is not…

What it is for

Purpose Pain reliever/ fever reducer

Key warnings

Warnings 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. Stomach bleeding warning: This product contains an NSAlD, which may cause severe stomach bleeding. The chance is higher if your child: ■ has had stomach ulcers or bleeding problems ■ takes a blood thinning (anticoagulant) or steroid drug ■ takes other drugs containing prescription or nonprescription…

Excerpts from the FDA label. Always read the leaflet in your pack and ask a pharmacist or doctor about your own situation.

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Recalls of this product

No FDA recalls are recorded for NDC 63941-128. Recalls are listed in FDA enforcement reports from 2004 onward.

Other recent recalls of ibuprofen

Same active ingredient, other companies or packs. Check the company and lot number on your pack.

Class II · Mar 25, 2026 · STRIDES PHARMA INC

Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.

Class II · Apr 16, 2025 · Glenmark Pharmaceuticals Inc., USA

CGMP Deviations

Class III · Nov 27, 2024 · Dr. Reddy's Laboratories, Inc.

Failed Tablet/Capsule Specifications

Class II · Sep 4, 2024 · Dr. Reddy's Laboratories, Inc.

Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.

Class II · Sep 4, 2024 · Dr. Reddy's Laboratories, Inc.

Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.

Class II · Sep 4, 2024 · Dr. Reddy's Laboratories, Inc.

Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.

Class II · Jun 15, 2022 · Mckesson Medical-Surgical Inc. Corporate Office

cGMP deviations: Temperature abuse

Class II · Jun 2, 2021 · Cardinal Health Inc.

CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Most reported side effects for ibuprofenReports to the FDA Adverse Event Reporting System (FAERS), all products with this ingredient
Drug ineffective27,693 reports
Pain19,680 reports
Fatigue19,019 reports
Nausea18,569 reports
Headache16,768 reports
Arthralgia13,653 reports
Dyspnoea13,291 reports
Vomiting13,216 reports
Diarrhoea12,902 reports
Dizziness11,570 reports
Show as table
ItemValue (reports)
Drug ineffective27,693
Pain19,680
Fatigue19,019
Nausea18,569
Headache16,768
Arthralgia13,653
Dyspnoea13,291
Vomiting13,216
Diarrhoea12,902
Dizziness11,570

These counts are reports, not proof that the medicine caused the problem. Popular medicines get more reports simply because more people take them. They are useful for spotting what to watch for, not for comparing medicines.

Official listing

Brand
Childrens Ibuprofen Oral Suspension, Dye Free
Generic name
IBUPROFEN
Company
Best Choice
Form
suspension
Route
oral
Type
HUMAN OTC DRUG
Category
ANDA
Listing valid to
Dec 31, 2026
Product NDC
63941-128

Active ingredients

Ibuprofen
100 mg/5mL

Packages (1)

The last part of the NDC identifies the pack size. Your box should show one of these.

63941-128-24 1 bottle in 1 carton (63941-128-24) / 118 ml in 1 bottle

Think your pack is fake?

Stop taking it, keep the pack and receipt, and show it to a pharmacist. In the U.S., report it to FDA MedWatch; elsewhere, to your national medicines regulator. How to spot a fake medicine.

Source: openFDA (U.S. Food and Drug Administration) drug directory, labels, enforcement reports and FAERS, retrieved Nov 10, 2026. The FDA notes this data should not be relied on alone for medical decisions. Not medical advice.