FDA.reportPublic FDA data

NDC 73656-012 - WHITE GLO CHARCOAL SENSITIVE

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
73656-012
Package NDCs from labels
73656-012-00
Manufacturer
WHITE GLO USA INC | Suzhou Baozi Healthy Technology Co.,Ltd
Effective date
2025-02-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SORBITOL - WHITE GLO USA INC | Suzhou Baozi Healthy Technology Co.,LtdWHITE GLO USA INC | Suzhou Baozi Healthy Technology Co.,Ltd2025-02-26HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73656-012-00WHITE GLO CHARCOAL SENSITIVE1 in 1 TUBEPASTE, DENTIFRICE50 mg in 1g6
73656-012-00WHITE GLO CHARCOAL SENSITIVE150 g in 1 BOXPASTE, DENTIFRICE150 g50 mg in 1g6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73656-012WHITE GLO CHARCOAL SENSITIVE (POTASSIUM NITRATE, SODIUM MONOFLUOROPHOSPHATE) KIT [WHITE GLO USA INC]6Unmatched20250228_a5edb7fd-c637-5447-e053-2995a90a5a6f.zip