Sodium Sulfacetamide 9% and Sulfur 4.5% Wash

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	82429-301	82429-301-21	D	Discontinued by firm		2026-10-15

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

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
82429-301-21	GM - Gram	82429-301	6af62a30-153e-4f1c-a71b-fdc7c07fc243	1	2022-11-07

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
82429-301	SODIUM SULFACETAMIDE 9% AND SULFUR 4.5% WASH (SULFACETAMIDE SODIUM AND SULFUR) RINSE [GABAR HEALTH SCIENCES CORP.]	3	Legacy NDC	20231022_82ffb2e9-0717-4094-8247-d3315eba0b0a.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4NRT660KJQ	SULFACETAMIDE SODIUM	6209-17-2	SULFACETAMIDE SODIUM
70FD1KFU70	SULFUR	7704-34-9	SULFUR

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
82429-301-21	82429030121	1 BOTTLE in 1 CARTON (82429-301-21) > 454 g in 1 BOTTLE	1 bottle	2022-10-10	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Sodium Sulfacetamide 9% and Sulfur 4.5% Wash	Gabar Health Sciences Corp.	2023-10-21	HUMAN PRESCRIPTION DRUG LABEL	3