Class III ยท Low risk
AllerClear D-24 hr
Failed Moisture Limits
National Drug Code
Is NDC 63981-0724-15 recalled?
KIRKLAND SIGNATURE ALLERCLEAR D 24 HR Extended Release · 1 BLISTER PACK in 1 CARTON (63981-724-15) / 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 63981-0724-15 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
- loratadine and pseudoephedrine sulfate
- Strength
- LORATADINE 10 mg/1; PSEUDOEPHEDRINE SULFATE 240 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Kirkland-COSTCO WHOLESALE COMPANY
- Type
- Human OTC Drug
- Product code
- 63981-0724
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
- 63981-0795 Severe Cold and Flu Plus Congestion 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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