NDC11 68016067414

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDCProduct root
68016-0674-1468016-0674
68016-674-1468016-674

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mucus Relief DM Maximum StrengthGUAIFENESIN, DEXTROMETHORPHAN HBRChain Drug Consortium, LLCd6aae1a1-0ab9-4b26-9f62-b8761014bb352025-06-30WarningsExact identifier
ndc (package): 68016-674-14
ndc (product): 68016-674
ndc11 (package): 68016067414

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.