Crest Pro-Health Sensitive and Gum All Day Protection

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 Pro-Health Sensitive and Gum All Day Protection
Generic name: STANNOUS FLUORIDE
Manufacturer: The Procter & Gamble Manufacturing Company
Product type: HUMAN OTC DRUG
SPL set ID: f4d775a1-a4f6-cd69-e053-2995a90a5f64
SPL ID: 47e317c2-ea4d-8cce-e063-6394a90a9182
Version: 9
Effective date: 2026-01-08
Source export date: 2026-10-27
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:49:59

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 1 of 1 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M021	openfda.application_number
brand name		Crest Pro-Health Sensitive and Gum All Day Protection	openfda.brand_name
generic name		STANNOUS FLUORIDE	openfda.generic_name
manufacturer name		The Procter & Gamble Manufacturing Company	openfda.manufacturer_name
ndc	package	69423-765-85	openfda.package_ndc
ndc	package	69423-765-52	openfda.package_ndc
ndc	package	69423-765-33	openfda.package_ndc
ndc	package	69423-765-03	openfda.package_ndc
ndc	package	69423-765-48	openfda.package_ndc
ndc	package	69423-765-28	openfda.package_ndc
ndc	package	69423-765-16	openfda.package_ndc
ndc	package	69423-765-41	openfda.package_ndc
ndc	package	69423-765-37	openfda.package_ndc
ndc	package	69423-765-46	openfda.package_ndc
ndc	product	69423-765	openfda.product_ndc
ndc11	package	69423076516	derived:openfda.package_ndc
ndc11	package	69423076585	derived:openfda.package_ndc
ndc11	package	69423076552	derived:openfda.package_ndc
ndc11	package	69423076546	derived:openfda.package_ndc
ndc11	package	69423076503	derived:openfda.package_ndc
ndc11	package	69423076537	derived:openfda.package_ndc
ndc11	package	69423076548	derived:openfda.package_ndc
ndc11	package	69423076528	derived:openfda.package_ndc
ndc11	package	69423076541	derived:openfda.package_ndc
ndc11	package	69423076533	derived:openfda.package_ndc
rxcui		416784	openfda.rxcui
spl id		47e317c2-ea4d-8cce-e063-6394a90a9182	id
spl set id		f4d775a1-a4f6-cd69-e053-2995a90a5f64	set_id
unii		3FTR44B32Q	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

Warnings When using this product do not use for sensitivity longer than four weeks unless recommended by a dentist. Stop use and ask a dentist if the sensitivity problem persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care. Keep out of reach of children. 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.