Darby

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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	66467-3790	66467-3790-1	D	Discontinued by firm		2026-07-31

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
sodium fluoride	ACTIVE INGREDIENT	8ZYQ1474W7	DARBY TOPICAL SODIUM FLUORIDE STRAWBERRY (SODIUM FLUORIDE) AEROSOL, FOAM [DARBY DENTAL SUPPLY CO]	2
fluoride ion	ACTIVE MOIETY	Q80VPU408O	DARBY TOPICAL SODIUM FLUORIDE STRAWBERRY (SODIUM FLUORIDE) AEROSOL, FOAM [DARBY DENTAL SUPPLY CO]	2

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
8ZYQ1474W7	SODIUM FLUORIDE	7681-49-4	SODIUM FLUORIDE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
66467-3790-1	66467379001	125 g in 1 BOTTLE, SPRAY (66467-3790-1)	125 g	2012-01-31	2021-12-31	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Darby Topical Sodium Fluoride Strawberry	Darby Dental Supply, LLC	2020-12-09	HUMAN PRESCRIPTION DRUG LABEL	6