NDC 83071-050-01 - Dr.Jucre Rebirth White

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
83071-050
Requested NDC
83071-050-01
Package NDCs from labels
83071-050-01, 83071-050-02
Manufacturer
NATURECELL CO., LTD. | Cosmax, Inc.
Effective date
2022-11-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Dr.Jucre Rebirth White - NATURECELL CO., LTD. | Cosmax, Inc.NATURECELL CO., LTD. | Cosmax, Inc.2022-11-08HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83071-050-022025-01-30C16284748780-12cef2736-9efa-d83d-e063-dadaa90ab31fda76b0a4-50cb-41f2-93a7-baaf55206221

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83071-050-01Dr.Jucre Rebirth White50 mL in 1 CONTAINERCREAM501
83071-050-02Dr.Jucre Rebirth White1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83071-050DR.JUCRE REBIRTH WHITE (NIACINAMIDE, ADENOSINE) CREAM [NATURECELL CO., LTD.]1Legacy NDC, 2 package rows20221109_da76b0a4-50cb-41f2-93a7-baaf55206221.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 35 of 35 · 681 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.