NDC 84712-001 - BARUBT BRIGHTENING

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
84712-001
Package NDCs from labels
84712-001-01
Manufacturer
Guangdong Youbaijia Cosmetic Industry Co., Ltd
Effective date
2024-09-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
BARUBT BRIGHTENING - Guangdong Youbaijia Cosmetic Industry Co., LtdGuangdong Youbaijia Cosmetic Industry Co., Ltd2024-09-04HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84712-001-01BARUBT BRIGHTENING20 g in 1 BOTTLECREAM201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84712-001BARUBT BRIGHTENING (BRIGHTENING) CREAM [GUANGDONG YOUBAIJIA COSMETIC INDUSTRY CO., LTD]11 package rows20240910_2157404b-ad43-f668-e063-6394a90a0458.zip