Class II · Moderate risk
Acetaminophen suspension liquid
Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
National Drug Code
Is NDC 30142-0590-26 recalled?
pain and fever
Yes — this exact package was recalled
1 FDA recall names the code 30142-0590-26 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
- acetaminophen
- Strength
- ACETAMINOPHEN 160 mg/5mL
- Form
- Suspension · Oral
- Labeler
- Kroger Company
- Type
- Human OTC Drug
- Product code
- 30142-0590
Recalls naming this package
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
- 30142-0388 nasal 3
- 30142-0600 See recall 3
- 30142-0766 infants pain and fever 3
- 30142-0810 70% Isopropyl Rubbing Alcohol 2
- 30142-0818 Childrens Pain and Fever 2
- 30142-0891 See recall 2
Free recall alerts
Know the day your medication is recalled
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