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 37808-0161-16 recalled?
Pain and Fever · 1 BOTTLE in 1 CARTON (37808-161-16) / 59 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 37808-0161-16 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
- H E B
- Type
- Human OTC Drug
- Product code
- 37808-0161
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
- 37808-0196 See recall 2
- 37808-0507 See recall 2
- 37808-0876 See recall 2
- 37808-0136 HEB Extra Stregth Antacid 1
- 37808-0288 See recall 1
- 37808-0305 HEB Antifungal 1
Free recall alerts
Know the day your medication is recalled
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