NDC11 42681903202

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
42681-9032-0242681-9032
42681-9032-242681-9032

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
365 Everyday Value Be Well Cough EaseANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, PONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIAWFM Private Label, LPd03ce312-2c79-4cc3-b6bf-3965aac136102023-03-16Exact identifier
ndc (package): 42681-9032-2
ndc (product): 42681-9032
ndc11 (package): 42681903202

Reported adverse events (FAERS/openFDA)#

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