NDC 71829-0002-1 - SpaGelpatch 42degrees celsius CORSET

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
71829-0002
Requested NDC
71829-0002-1
Package NDCs from labels
71829-0002-1, 71829-0002-2
Manufacturer
SENNY STUDIO Co., Ltd
Effective date
2017-11-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SpaGelpatch 42degrees celsius CORSET - SENNY STUDIO Co., LtdSENNY STUDIO Co., Ltd2017-11-20HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71829-0002-22020-01-31C16284748780-19d75b9d0-16e7-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71829-0002-1SpaGelpatch 42degrees celsius CORSET7.6 g in 1 PATCHPATCH7.61
71829-0002-2SpaGelpatch 42degrees celsius CORSET5 in 1 PACKAGEPATCH51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71829-0002SPAGELPATCH 42DEGREES CELSIUS CORSET (CAPSICUM ANNUUM WHOLE) PATCH [SENNY STUDIO CO., LTD]12 package rows20171121_5e766544-48df-050d-e053-2991aa0aafa7.zip

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 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Comfort Down There HemorrhoidsAESCULUS HIPPOCASTANUM 5C, ALOE 5C, BERBERIS VULGARIS 3C, CAPSICUM ANNUUM 5C, CARDUUS MARIANUS 3C, NUX VOMICA 5C, PULSATILLA 9CSEVENE USA55001764-8bc9-cbac-e063-6394a90a455c2026-08-18WarningsExact identifier
unii: 7FKZ3QQQ1F
5e766544-48e0-050d-e053-2991aa0aafa75e766544-48df-050d-e053-2991aa0aafa72017-11-20WarningsExact identifier
spl id: 5e766544-48e0-050d-e053-2991aa0aafa7
spl set id: 5e766544-48df-050d-e053-2991aa0aafa7

Reported adverse events (FAERS/openFDA)#

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