Crest Tartar Protection

Product NDC
58933-009
11-digit product format
589330009
Labeler code
58933
Product ID
58933-009_c46d2edc-404c-7e08-e053-2995a90a043c
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium Fluoride
Dosage form
GEL, DENTIFRICE
Route
DENTAL
Labeler
Procter & Gamble Manufactura, S. de R.L. de C.V.
Application
part355
Marketing category
OTC MONOGRAPH FINAL
Marketing start
1995-06-16
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct58933-009DDiscontinued by firm2026-10-15
excluded packagepackage58933-00958933-009-62DDiscontinued by firm2026-10-15

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58933-009CREST TARTAR PROTECTION FRESH MINT GEL (SODIUM FLUORIDE) GEL, DENTIFRICE [PROCTER & GAMBLE MANUFACTURA, S. DE R.L. DE C.V.]5Legacy NDC20250110_597b01a5-b186-6948-e053-2991aa0aab70.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58933-009-62589330009621 TUBE in 1 CARTON (58933-009-62) > 175 g in 1 TUBE1 tube1995-06-160000-00-00NoNoCurrent