Sulfur 30 Special Order

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	48951-8220	48951-8220-3	I	Inactivated by FDA		2026-10-15

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

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8220-3	Sulfur 30 Special Order	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		2

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SULFUR	ACTIVE INGREDIENT	70FD1KFU70	SULFUR 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1
SULFUR	ACTIVE MOIETY	70FD1KFU70	SULFUR 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	SULFUR 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8220	SULFUR 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	2	Legacy NDC, 1 package rows	20180501_75259cb9-9a45-48fe-9103-38a485dc85ea.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
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
48951-8220-3	48951822003	60 mL in 1 BOTTLE, DROPPER (48951-8220-3)	60 ml	2009-09-01	0000-00-00	No	No	Current