Crest Complete plus

Product NDC: 37000-956
Requested package NDC: 37000-956-54
11-digit product format: 370000956
Labeler code: 37000
Product ID: 37000-956_c68af5cc-7e55-0d2c-e053-2995a90ad917
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Fluoride
Dosage form: PASTE, DENTIFRICE
Route: DENTAL
Labeler: The Procter & Gamble Manufacturing Company
Application: part355
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2020-01-01
Marketing end: 0000-00-00
Substance: SODIUM FLUORIDE
Active strength: 2 mg/g
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	37000-956	37000-956-54	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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	37000-956	37000-956-54	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	37000-956	37000-956-54	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
37000-956-06	2023-03-31	Crest ® Complete plus™ +WHITENING CINNAMON EXPRESSIONS
37000-956-54	2023-03-31	Crest ® Complete plus™ +WHITENING CINNAMON EXPRESSIONS
37000-956-06	2023-01-30	Crest ® Complete plus™ +WHITENING CINNAMON EXPRESSIONS
37000-956-54	2023-01-30	Crest ® Complete plus™ +WHITENING CINNAMON EXPRESSIONS

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37000-956	CREST COMPLETE PLUS WHITENING CINNAMON EXPRESSIONS (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	7	Legacy NDC	20250110_9fa60007-530d-3ebf-e053-2a95a90a3450.zip

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
37000-956-54	37000095654	1 TUBE in 1 CARTON (37000-956-54) > 153 g in 1 TUBE	1 tube	2020-06-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Crest ® Complete plus™ +WHITENING CINNAMON EXPRESSIONS	The Procter & Gamble Manufacturing Company	2025-01-08	HUMAN OTC DRUG LABEL	7