NDC 70758-020-01 - REPIEL SMART NAIL PACK MIRACLE BUTTER

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
70758-020
Requested NDC
70758-020-01
Package NDCs from labels
70758-020-01, 70758-020-02
Manufacturer
THE COSRISE CO.,LTD
Effective date
2016-06-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
REPIEL SMART NAIL PACK MIRACLE BUTTER - THE COSRISE CO.,LTDTHE COSRISE CO.,LTD2016-06-29HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70758-020-022021-01-29C16284748780-1ba0f9c33-406e-a910-e053-dadaa90a0b85b709fde3-523d-4749-bd4d-05e0fa4814fa

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70758-020-01REPIEL SMART NAIL PACK MIRACLE BUTTER3 mL in 1 POUCHPATCH31
70758-020-02REPIEL SMART NAIL PACK MIRACLE BUTTER10 in 1 CARTONPATCH101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70758-020REPIEL SMART NAIL PACK MIRACLE BUTTER (GLYCERIN) PATCH [THE COSRISE CO.,LTD]1Legacy NDC, 2 package rows20160629_b709fde3-523d-4749-bd4d-05e0fa4814fa.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 29 of 29 · 561 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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