Crest Premium Plus Sensitivity Active Foam

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 Premium Plus Sensitivity Active Foam
Generic name: SODIUM FLUORIDE AND POTASSIUM NITRATE
Manufacturer: The Procter & Gamble Manufacturing Company
Product type: HUMAN OTC DRUG
SPL set ID: b8535d1c-cf15-f353-e053-2a95a90a7974
SPL ID: 47e4e251-448a-efc5-e063-6294a90a56a8
Version: 12
Effective date: 2026-01-08
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:47

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M021	openfda.application_number
brand name		Crest Premium Plus Sensitivity Active Foam	openfda.brand_name
generic name		SODIUM FLUORIDE AND POTASSIUM NITRATE	openfda.generic_name
manufacturer name		The Procter & Gamble Manufacturing Company	openfda.manufacturer_name
ndc	package	37000-995-52	openfda.package_ndc
ndc	package	37000-995-70	openfda.package_ndc
ndc	product	37000-995	openfda.product_ndc
ndc11	package	37000099570	derived:openfda.package_ndc
ndc11	package	37000099552	derived:openfda.package_ndc
rxcui		1038800	openfda.rxcui
spl id		47e4e251-448a-efc5-e063-6294a90a56a8	id
spl set id		b8535d1c-cf15-f353-e053-2a95a90a7974	set_id
unii		8ZYQ1474W7	openfda.unii
unii		RU45X2JN0Z	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 longer than four weeks unless recommended by a dentist. Stop use and ask a dentist if problem lasts or gets worse. 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.