NDC 73656-021 - White Glo Activated Charcoal Twin Pack

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: 73656-021
Package NDCs from labels: 73656-021-00
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
SODIUM FLUORIDE - 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
73656-021	WHITE GLO ACTIVATED CHARCOAL TWIN PACK (SODIUM FLUORIDE) KIT [WHITE GLO USA INC]	5	Unmatched	20250228_6adaca4f-5599-41e0-9215-c7ee5c1dc372.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 83 of 91 · 1,820 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Family Wellness HEMORRHOID	GLYCERIN, PETROLATUM, PHENYLEPHRINE HCL, PRAMOXINE HCL	FAMILY DOLLAR (Family Wellness)	16ceb129-5c0a-428a-a867-cfbbb08bb62a	2023-12-11	Warnings	Exact identifier unii: PDC6A3C0OX
La Roche Posay Laboratoire Dermatologique Cicaplast Defense B5	GLYCERIN	Cosmetique Active Production	01c8a0d5-bcd1-4639-be45-530a226401f0	2023-12-11	Warnings	Exact identifier unii: PDC6A3C0OX
Hemorrhoidal Pain Relief Cream	GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM	WALGREENS	03bbe146-f185-bcfa-e063-6394a90a85bf	2023-12-04	Warnings	Exact identifier unii: PDC6A3C0OX
Eye Wash	WATER	Jiangxi Zhenmei Biological Technology Co.,Ltd	c68795b8-bf68-0d01-e053-2a95a90abebb	2023-12-04	Warnings	Exact identifier unii: 059QF0KO0R
Bloop Hemorrhoid Relief Topical	GLYCERIN, PETROLATUM, PHENYLEPHRINE HCL, PRAMOXINE HCL	Three Nations Corp	0b6419e3-f1c7-bdfe-e063-6294a90a5d92	2023-11-30	Warnings	Exact identifier unii: PDC6A3C0OX
Beyond Activated Coconut Charcoal and Sea Salt	SODIUM FLUORIDE	Beyond International Inc	d075fa15-7309-0c10-e053-2995a90a7c95	2023-11-28	Warnings	Exact identifier application number: M021
Pro-Den Rx	STANNOUS FLUORIDE	Den-mat Holdings, Llc	9036aa8a-59b1-41b0-b3cb-529d3303a1c0	2023-11-20	Warnings	Exact identifier application number: M021
Fluoridex	STANNOUS FLUORIDE RINSE	DEN-MAT HOLDINGS, LLC	5e81f073-c0ca-aa38-e053-2a91aa0ab37b	2023-11-20	Warnings	Exact identifier application number: M021
Hello Vitamin C Whitening	SODIUM FLUORIDE	Colgate-Palmolive Company	38a0276e-910c-527d-1736-65928b9d4ca4	2023-11-20	Warnings	Exact identifier application number: M021
POP Feeling Peachy	SODIUM FLUORIDE	LG H&H CO., LTD.	0abaf99b-9547-46ae-e063-6394a90a6c15	2023-11-17	Warnings	Exact identifier application number: M021
UNIVERSAL ANTI-CAVITY FLUORIDE	SODIUM MONOFLUOROPHOSPHATE	Universal Distribution Center LLC	e3356374-befa-41b0-ab0f-edfd5a062601	2023-11-16	Warnings	Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q
ANTI CAVITY FLUORIDE	SODIUM MONOFLUOROPHOSPHATE	Universal Distribution Center LLC	421fc2f0-b118-4e7a-a399-ba4780028c54	2023-11-16	Warnings	Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q
UNIVERSAL CHARCOAL WITH ALOE VERA ANTI-CAVITY FLUORIDE	SODIUM FLUORIDE	Universal Distribution Center LLC	3411924d-1002-460c-83e8-c0c7fbff9ad1	2023-11-16	Warnings	Exact identifier application number: M021
ADVANCED WHITENING ANTI CAVITY FLUORIDE	SODIUM MONOFLUOROPHOSPHATE	Universal Distribution Center LLC	8ea8a8d9-b7e4-468f-9a09-4ec634cbd80e	2023-11-16	Warnings	Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q
UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE	SODIUM MONOFLUOROPHOSPHATE	Universal Distribution Center LLC	879dfaf0-27c8-41a3-8d01-a1c3eec9edfc	2023-11-15	Warnings	Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q
Gun powder	POTASSIUM NITRATE, ACTIVATED CHARCOAL, SULFUR	Boiron	a7aa3ac0-beec-11e7-81f2-424c58303031	2023-11-13		Exact identifier unii: 2P3VWU3H10
Gun powder	POTASSIUM NITRATE, ACTIVATED CHARCOAL, SULFUR	Boiron	85cb268d-43b4-3c6e-e053-2991aa0a050f	2023-11-13		Exact identifier unii: 2P3VWU3H10
Carbo vegetabilis	ACTIVATED CHARCOAL	Boiron	84a034a4-4504-2148-e053-2991aa0a02af	2023-11-09		Exact identifier unii: 2P3VWU3H10
Carbo vegetabilis	ACTIVATED CHARCOAL	Boiron	8517edac-fd8f-7a49-e053-2a91aa0a24cd	2023-11-09		Exact identifier unii: 2P3VWU3H10
Carbo vegetabilis	ACTIVATED CHARCOAL	Boiron	84a0cc39-edf0-8407-e053-2991aa0a12dc	2023-11-09		Exact identifier unii: 2P3VWU3H10

Reported adverse events (FAERS/openFDA)#

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