Whitening Kit

Product NDC: 51316-410
11-digit product format: 513160410
Labeler code: 51316
Product ID: 51316-410_d0701007-80bc-156b-e053-2a95a90ab985
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium MFP
Dosage form: KIT
Labeler: CVS
Application: part356
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2021-11-09
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	51316-410		D	Discontinued by firm		2026-10-05
excluded package	package	51316-410	51316-410-09	D	Discontinued by firm		2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	51316-410-09	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	51316-410-09	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	51316-410-09	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51316-410-09	2024-02-12	C162847	48780-1	f386c649-e9b0-0266-e053-dadaa90a7c1a	5820410 CVS Weekend White Kit
51316-410-09	2023-01-30	C162847	48780-1	f386c649-e9b0-0266-e053-dadaa90a7c1a	5820410 CVS Weekend White Kit

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
51316-410-09	51316041009	1 KIT in 1 CARTON (51316-410-09) * 76.5 g in 1 TUBE	1 kit	2021-11-09	0000-00-00	No	No	Current