NDC 73199-0003 - BOTANETH PRONOXIN HAIR REGAINER FS2 ACTIVATOR 2-A 2-B

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
73199-0003
Package NDCs from labels
73199-0003-1
Manufacturer
OUIBON GLOBAL | LABIO Co., Ltd.
Effective date
2019-07-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Drug FactsOUIBON GLOBAL | LABIO Co., Ltd.2019-07-13HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73199-0003-1BOTANETH PRONOXIN HAIR REGAINER FS2 ACTIVATOR 2-A 2-B60 mL in 1 BOTTLE, PLASTICLIQUID60 mL0.1 g in 100mL1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73199-0003BOTANETH PRONOXIN HAIR REGAINER FS2 ACTIVATOR 2-A 2-B (ALLANTOIN) KIT [OUIBON GLOBAL]1Unmatched20190713_8d8bbfdf-4fa5-2c77-e053-2995a90ab11e.zip