NDC 73656-010 - WHITE GLO CHARCOAL

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: 73656-010
Package NDCs from labels: 73656-010-00
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
Label	Manufacturer	Effective date	Type
WHITE GLO CHARCOAL - WHITE GLO USA INC \| Suzhou Baozi Healthy Technology Co.,Ltd	WHITE GLO USA INC \| Suzhou Baozi Healthy Technology Co.,Ltd	2025-02-26	HUMAN OTC DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73656-010	WHITE GLO CHARCOAL (SODIUM MONOFLUOROPHOSPHATE) KIT [WHITE GLO USA INC]	5	Unmatched	20250228_a14bb838-f07a-3a6f-e053-2995a90a535d.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 118 of 118 · 2,342 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Eagle Brand Medicated Oil Aromatic	CAMPHOR, MENTHOL, METHYL SALICYLATE	Borden Company (Private) Limited	54e45d89-e8c3-6fc3-e063-6394a90aac4e	2015-06-15	Warnings	Exact identifier unii: LAV5U5022Y

Reported adverse events (FAERS/openFDA)#

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