NDC 60764-050-01 - 3CE LIP COLOR 906 BITE IT

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
60764-050
Requested NDC
60764-050-01
Package NDCs from labels
60764-050-01, 60764-050-02
Manufacturer
Nanda Co., Ltd | Cosmax, Inc.
Effective date
2016-09-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
3CE LIP COLOR 906 BITE IT - Nanda Co., Ltd | Cosmax, Inc.Nanda Co., Ltd | Cosmax, Inc.2016-09-30HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60764-050-022020-01-31C16284748780-19d75b9cf-de11-f424-e053-dadaa90a57cece2c6759-429b-45fd-abb1-59f160a0030a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60764-050-013CE LIP COLOR 906 BITE IT3.5 g in 1 BOTTLELIPSTICK3.51
60764-050-023CE LIP COLOR 906 BITE IT1 in 1 CARTONLIPSTICK11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60764-0503CE LIP COLOR 906 BITE IT (TRIETHYLHEXANOIN) LIPSTICK [NANDA CO., LTD]1Legacy NDC, 2 package rows20160930_ce2c6759-429b-45fd-abb1-59f160a0030a.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 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
9f5df684-5b99-4010-bed1-e6a1e5792574ce2c6759-429b-45fd-abb1-59f160a0030a2016-09-30WarningsExact identifier
spl id: 9f5df684-5b99-4010-bed1-e6a1e5792574
spl set id: ce2c6759-429b-45fd-abb1-59f160a0030a

Reported adverse events (FAERS/openFDA)#

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