Crest Pro-Health Stages

Product NDC
58933-673
11-digit product format
589330673
Labeler code
58933
Product ID
58933-673_9999ea24-c298-cfa4-e053-2a95a90a3694
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium Fluoride
Dosage form
PASTE, DENTIFRICE
Route
DENTAL
Labeler
Procter & Gamble Manufactura, S. de R.L. de C.V.
Application
part355
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2008-08-01
Marketing end
2021-12-01
Substance
SODIUM FLUORIDE
Active strength
2 mg/g
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct58933-673DDiscontinued by firm2026-07-31
excluded packagepackage58933-67358933-673-04DDiscontinued by firm2026-07-31

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Plus WhiteSODIUM MONOFLUOROPHOSPHATECCA Industries, Inc.7581b27b-6acb-45b0-8804-b5dae34989312018-08-01WarningsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

Warnings If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58933-673-0458933067304120 g in 1 TUBE (58933-673-04) 120 g2008-08-012021-12-01NoNoCurrent