NDC 0363-6171-09 Walgreens Sinus Pressure — Class III drug recall D-0014-2023
Terminated recall by LNK International, Inc., reported 2022-10-26, distributed nationwide. Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg
| Recall number | D-0014-2023 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | LNK International, Inc., Hauppauge, NY, United States |
| Recall initiated | 2022-10-11 |
| Classified | 2022-10-18 |
| Reported by FDA | 2022-10-26 |
| Terminated | 2023-07-25 |
| Distributed | Nationwide (US) |
| Quantity | 66,384 boxes |
| Reason classes | labeling |
| NDC | 00363-6171, 00363-6171-09 |
Product
NDC 0363-6171-09 Walgreens Sinus Pressure, Pain & Cough ACETAMINOPHEN/ PAIN RELIEVER DEXTROMETHORPHAN HBr/ COUGH SUPPRESSANT GUAIFENESIN/ EXPECTORANT PHENYLEPHRINE HCl/ NASAL DECONGESTANT Maximum Strength Decongestant Free DISTRIBUTED BY: WALGREENS CO. 200 WILMOT RD., DEERFIELD, IL 60015 walgreens.com
Reason for recall
Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0014-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.