Class II · Moderate risk
POLYETHYLENE GLYCOL 3350 Powder for Solution Osmotic Laxative 14…
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 45802-0868-66 recalled?
Polyethylene Glycol 3350 · 14 PACKET in 1 CARTON (45802-868-66) / 17 g in 1 PACKET
Yes — this exact package was recalled
1 FDA recall names the code 45802-0868-66 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
- Polyethylene Glycol 3350
- Strength
- POLYETHYLENE GLYCOL 3350 17 g/17g
- Form
- Powder, for Solution · Oral
- Labeler
- Padagis Israel Pharmaceuticals Ltd
- Type
- Human OTC Drug
- Product code
- 45802-0868
Recalls naming this package
Class II · Moderate risk
Polyethylene Glycol 3350 Powder for Solution
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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
- 45802-0425 See recall 2
- 45802-0571 See recall 2
- 45802-0014 Hydrocortisone 1
- 45802-0054 Triamcinolone Acetonide 1
- 45802-0059 Nystatin 1
- 45802-0063 Triamcinolone Acetonide 1
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.