FDA.reportPublic FDA data

NDC11 42829040101

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
42829-0401-0142829-0401
42829-0401-142829-0401
42829-401-0142829-401

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 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SinuCleanse Neti-PotSODIUM BICARBONATE, SODIUM CHLORIDEASCENT CONSUMER PRODUCTS, INC.ba953a99-4885-4823-9905-75ce3eae160c2025-01-31WarningsExact identifier
ndc (package): 42829-401-01
ndc11 (package): 42829040101
SinuCleanse SqueezeSODIUM BICARBONATE, SODIUM CHLORIDEASCENT CONSUMER PRODUCTS, INC.e8f7ea0b-0838-40ac-af1c-6a5ca7afbebe2025-01-31WarningsExact identifier
ndc (package): 42829-401-01
ndc11 (package): 42829040101
SinuCleanseSODIUM BICARBONATE, SODIUM CHLORIDEASCENT CONSUMER PRODUCTS, INC.c33bf872-54aa-45e0-9e40-a6565a13f1982025-01-31WarningsExact identifier
ndc (package): 42829-401-01
ndc (product): 42829-401
ndc11 (package): 42829040101

Reported adverse events (FAERS/openFDA)#

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