Crest 3D White Radiant Mint

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Crest 3D White Radiant Mint
Generic name: SODIUM FLUORIDE
Manufacturer: The Procter & Gamble Manufacturing Company
Product type: HUMAN OTC DRUG
SPL set ID: f3dd7a34-a0d8-4ac6-bbd1-7c3b86187a57
SPL ID: 47e4b8ca-c352-d5c6-e063-6294a90a50c2
Version: 21
Effective date: 2026-01-08
Source export date: 2026-10-12
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:28:45

Harmonized routes table
Harmonized routes
DENTAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 2 of 2 · 47 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
ndc11	package	37000087630	derived:openfda.package_ndc
ndc11	package	37000087602	derived:openfda.package_ndc
ndc11	package	37000087605	derived:openfda.package_ndc
rxcui		891775	openfda.rxcui
spl id		47e4b8ca-c352-d5c6-e063-6294a90a50c2	id
spl set id		f3dd7a34-a0d8-4ac6-bbd1-7c3b86187a57	set_id
unii		8ZYQ1474W7	openfda.unii

Warnings cross-check#

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

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warning Keep out of reach of children under 6 yrs. of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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