Licorice Coughing Liquid — Class I drug recall D-0908-2016
Terminated recall by Master Herbs, Inc./Li, reported 2016-06-01, distributed nationwide. Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.
| Recall number | D-0908-2016 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Master Herbs, Inc./Li, Pomona, CA, United States |
| Recall initiated | 2016-01-15 |
| Classified | 2016-05-26 |
| Reported by FDA | 2016-06-01 |
| Terminated | 2017-02-07 |
| Distributed | Nationwide (US) |
| Quantity | 6,024 bottles |
| Reason classes | undeclared allergen, unapproved product |
| NDC | 68511-0460-01 |
Product
Licorice Coughing Liquid (guaifenesin), 5%, 3.38 fl. oz. (100 ml), OTC, Manufactured by: Ma Ying Long Pharmaceutical Group Co., LTD, Wuhan, China; Distributed by: Master Herbs (USA) Inc., NDC 68511-0460-01
Reason for recall
Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.
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-0908-2016. 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.