Class II ยท Moderate risk
Kirkland Severe Cold & Flu Plus Congestion: Day - 112 coated caplets blister pack
CGMP Deviations: Released product should have been rejected.
National Drug Code
Is NDC 63981-0795-81 recalled?
Severe Cold and Flu Plus Congestion · 14 BLISTER PACK in 1 CARTON (63981-795-81) / 1 KIT in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 63981-0795-81 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, Dextromethorphan HBr, Doxylamine succinate, Guaifenesin, Phenylephrine HCl
- Form
- Kit
- Labeler
- Costco Wholesale Corporation
- Type
- Human OTC Drug
- Product code
- 63981-0795
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
- 63981-0171 Kirkland Ultra Stregth Antacid 171AB 1
- 63981-0571 See recall 1
- 63981-0724 KIRKLAND SIGNATURE ALLERCLEAR D 24 HR Extended Release 1
- 63981-0847 kirkland signature aller fex 1
- 63981-0852 See recall 1
Free recall alerts
Know the day your medication is recalled
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