Class II · Moderate risk
Children's Ibuprofen Oral Suspension USP
Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing.
National Drug Code
Is NDC 51672-2130-01 recalled?
Ibuprofen · 1 BOTTLE in 1 CARTON (51672-2130-1) / 240 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 51672-2130-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Ibuprofen
- Strength
- IBUPROFEN 100 mg/5mL
- Form
- Suspension · Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human OTC Drug
- Product code
- 51672-2130
Recalls naming this package
Class II · Moderate risk
Children's Ibuprofen Oral Suspension USP
Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing.
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 51672-1386 Fluocinonide 3
- 51672-1351 Ciclopirox 2
- 51672-1385 Ibuprofen 2
- 51672-3007 Hydrocortisone and Acetic Acid 2
- 51672-4005 Carbamazepine 2
- 51672-4027 Warfarin Sodium 2
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.