Class II · Moderate risk
Guaifenesin USP
Presence of Foreign Matter: Guaifenesin API powder is being recalled due to the possibility that the product contains polyethylene fibers from a screen used to sift the Guaifenesin.
National Drug Code
Is NDC 60203-1001 recalled?
Guaifenesin
This product was recalled — in other package sizes
No FDA recall names your exact package code, but 1 recall cover the same product (60203-1001) in a different bottle or carton size. Worth checking with your pharmacist.
- Active ingredient
- Guaifenesin
- Strength
- GUAIFENESIN 1 kg/kg
- Form
- Powder
- Labeler
- Delta Synthetic Co. Ltd
- Type
- Bulk Ingredient
- Product code
- 60203-1001
Recalls of this product
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.
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.